The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of projects in terms of quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory and organizational standards.
The Assistant CRA provides remote support for clinical trial site preparedness, monitoring processes, and study management tasks. They coordinate site documentation, supply management, and system access while ensuring compliance with regulatory guidelines and SOPs.
You will develop and execute comprehensive talent acquisition strategies to support global organizational growth and mission-driven hiring. This role involves collaborating with business leaders to implement recruiting solutions, manage diversity initiatives, and utilize market intelligence to optimize hiring processes.
The Regulatory Affairs Manager will own regulatory decision-making for clinical programs and drive cross-functional teams to execute regulatory strategies. They are responsible for providing strategic intelligence, ensuring compliance with global requirements, and managing client interfaces throughout the product development lifecycle.
The Senior Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits, manage documentation, and mentor junior team members to maintain audit readiness.
The Digital Account Manager will drive revenue growth and customer retention across a large portfolio of accounts in the Nordics using a digital-first approach. They will manage a sales pipeline, engage customers through various digital channels, and collaborate with cross-functional teams to optimize the online customer journey.
The Senior Regulatory Affairs Specialist will lead global regulatory strategies for clinical trials and act as a primary liaison between internal teams and external clients. They are responsible for preparing regulatory submissions, providing strategic guidance, and ensuring compliance with global regulatory guidelines.
The Clinical Trial Manager is responsible for achieving clinical deliverables within time, quality, and cost expectations while managing study operations and quality aspects. They lead clinical teams, ensure compliance with ICH GCP, and manage project financials and resource allocation.
The Senior Clinical Team Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, manage project financials, and ensure compliance with ICH GCP and regulatory standards.
The Biostatistician II functions as a lead statistician to deliver analysis databases, statistical analyses, and formatted summaries while mentoring junior team members. They also lead project teams, coordinate with data management personnel, and ensure compliance with SOPs and project timelines.
The Senior Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They facilitate communication between investigative sites and the project team while managing trial documentation and site initiation activities.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage essential documentation to maintain audit readiness.
The Associate Director provides senior operational leadership for a portfolio of registries and real-world evidence programs, translating commitments into coordinated delivery plans. They oversee operational performance, manage risks, and align cross-functional teams, vendors, and client stakeholders to ensure program success.
The Associate Clinical Manager oversees daily line management, coaching, and professional development for clinical operations staff. They also collaborate with senior management on strategic planning, resourcing, and ensuring adherence to clinical trial SOPs and regulatory standards.
The Technical Sales Specialist is responsible for driving revenue growth by selling and supporting ICP-OES and ICP-MS instrumentation across the Western United States and Canada. This role involves identifying new business opportunities, providing technical expertise to customers, and collaborating with internal teams to deliver comprehensive analytical solutions.
The role serves as the functional and configuration lead for Workday Time Tracking and Absence implementations, managing project workstreams from requirements through deployment. It involves coordinating cross-functional teams and stakeholders to deliver scalable solutions that meet complex payroll and regulatory requirements.
The Senior Clinical Research Associate I performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They act as a representative of the client, conducting remote or on-site visits and managing essential documentation in accordance with ICH-GCP guidelines.
The Patient Data Specialist performs critical assessments of clinical trial data to identify trends, risks, and areas for optimization. They lead interdepartmental discussions to define study-specific setups and ensure data compatibility with downstream systems.
The Assistant CRA provides remote support for clinical trial site preparedness, monitoring processes, and site management tasks. They ensure compliance with SOPs and regulatory guidelines while coordinating study-specific documentation and logistics.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Facilitates communication between investigative sites, the client, and internal teams while managing clinical trial documentation and site processes.
The Senior Systems Analyst will coordinate complex HR technology initiatives, including Workday enhancements, M&A integrations, and strategic projects. They are responsible for gathering requirements, managing testing strategies, and ensuring seamless delivery across functional and technical workstreams.
The Senior Systems Analyst will coordinate complex Workday and HR technology initiatives, including M&A integrations and system enhancements. They are responsible for gathering requirements, managing project workstreams, and leading end-to-end testing strategies to ensure successful deployment.
The Sr. Systems Analyst will serve as a functional lead for Workday Time and Absence implementations during M&A and strategic HR technology projects. They are responsible for designing configurations, managing functional workstreams, and ensuring successful system integration and stabilization.
You will lead statistical tasks throughout the clinical trial process, including study design, protocol writing, and final analysis. Additionally, you will collaborate with scientific experts to advance research and ensure high-quality reporting for clinical development programs.
The Sr Sales Training Manager is responsible for the design, development, and delivery of comprehensive training programs for the Pharma Services Group commercial sales teams. This role involves leveraging blended learning approaches, managing training platforms, and collaborating cross-functionally to ensure training initiatives align with business outcomes.
Responsible for the installation, maintenance, qualification, and repair of liquid and ion chromatography systems coupled with mass spectrometers. Provides technical support to customers and assists in the development of service documentation and quality reports.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also manage study documentation, facilitate cross-functional communication, and assist with process improvements and site-level coordination.
Lead the technical delivery of AI projects by defining solution architecture, implementation plans, and integrating AI applications into finance business processes. Collaborate with cross-functional teams to identify valuable use cases, mentor junior staff, and ensure the reliability and scalability of deployed AI solutions.
The role involves orchestrating RFP strategies, developing client proposals, and negotiating contracts to secure new business. You will also maintain client relationships, conduct cold calls, and ensure high levels of client satisfaction.
You will handle inbound customer calls and emails to resolve requests regarding pricing, product availability, returns, and delivery. Additionally, you will collaborate with international teams to ensure high standards of customer satisfaction and build strong stakeholder relationships.
Provide strategic statistical expertise and oversight for clinical research programs, including Phase IIIb/IV trials and observational studies. Act as a key statistical representative on cross-functional teams to support evidence-generation strategies and regulatory submissions.
The Principal Regulatory Affairs Specialist will lead global regulatory strategies for clinical trials and act as a primary liaison with internal and external clients. They are responsible for managing project teams, preparing regulatory submissions, and providing strategic regulatory intelligence.
You will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Additionally, you will provide tailored scientific solutions through consultative selling and cross-functional collaboration.
Develop and implement strategic sales plans while managing key account relationships within the Biotech sector. Provide tailored scientific solutions through consultative selling and virtual engagement to meet sales targets.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
Provides administrative, contractual, and financial support for processing payments to investigative sites. Ensures adherence to country-specific regulations and manages relationships with study sites to resolve payment-related issues.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
The Senior Product Specialist will support revenue growth and customer success by applying technical expertise and a consultative sales approach. They will provide technical leadership in customer engagements, conduct product demonstrations, and serve as a trusted advisor to help customers achieve research goals.
The Project Manager leads and coordinates central laboratory activities across clinical trial programs to ensure project performance and client satisfaction. They act as the primary liaison between sponsors and internal departments while overseeing study initiation, protocol management, and regulatory compliance.
The Vice President will lead the global commercial strategy for the Bioanalytical and Biomarker Laboratories business to drive profitable growth and market expansion. They will transform the commercial model from reactive fulfillment to proactive demand generation while building high-performing teams and strategic customer partnerships.
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. This includes leading clinical teams, monitoring study performance, and ensuring compliance with ICH GCP and regulatory standards.
You will develop and implement business development strategies to identify and pursue new opportunities within the CBRNe Safety & Security industry. This role involves managing the full sales cycle from lead generation to contract negotiation while building strategic partnerships with Federal and State agencies.
The Associate Clinical Data Team Lead II supports lead data managers by performing study setup, data cleaning, and database close-out tasks. They also mentor junior staff, monitor study metrics, and ensure project deliverables meet quality standards.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of assigned studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory standards throughout the project lifecycle.
Install, maintain, troubleshoot, and repair advanced analytical instrumentation such as OES, XRF, and XRD systems at customer sites. Manage service calls, parts inventory, and provide technical training to customers and colleagues.
The Clinical Trial Coordinator provides administrative and technical support to project teams, including managing trial documentation and site activation activities. They ensure clinical systems are accurate, maintain tracking tools, and coordinate with suppliers to support trial execution.
The Field Service Engineer will install, maintain, troubleshoot, and repair complex analytical and scientific instruments in various laboratory settings. They are responsible for providing exceptional customer service and training clients on equipment operation while documenting all service activities.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing complex analytical and scientific instruments. They will provide exceptional customer service and support while ensuring all work adheres to safety and quality standards.
Provides administrative and technical support to the project team by coordinating trial activities and maintaining study documentation. Ensures tasks are completed on time and within budget while acting as a cross-functional liaison for project initiatives.
You will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring activities. Additionally, you will manage site documentation, facilitate communication between stakeholders, and ensure trial readiness for audits.
Conduct remote or on-site monitoring visits to assess protocol and regulatory compliance, manage trial documentation, and coordinate clinical monitoring and site management activities. Ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and standard operating procedures while maintaining audit readiness and collaborative relationships with investigational sites.
Coordinates clinical trial and site activation activities, maintains study systems and documentation, and supports regulatory submissions, feasibility, and audit readiness. Tracks project tasks and risks, communicates with sites and internal teams, and helps ensure work meets timelines, quality standards, and applicable procedures.
The Senior Regulatory Affairs Specialist will provide strategic regulatory guidance and manage global clinical trial transparency deliverables, including protocol registration and document redaction. They will act as a liaison between internal and external clients to ensure compliance with global regulatory requirements throughout the product lifecycle.
The Regulatory Affairs Manager will provide strategic regulatory intelligence and guidance to support product development from preclinical stages through registration. They will monitor global regulatory developments, assess their impact on client pipelines, and act as a subject matter expert to cross-functional teams.
The Director provides senior technical and operational leadership for CMC regulatory services, overseeing FSP teams and client engagements. They are responsible for resource planning, business development support, and ensuring high-quality, compliant delivery across all projects.
Design and implement health economic simulation models to assess the cost-effectiveness of healthcare interventions. Manage project timelines, budgets, and deliverables while mentoring junior staff and supporting the Principal Investigator.
The Account Development Analyst supports RFP funnel growth by researching prospective client pipelines and identifying qualified leads. They also manage marketing-generated leads, provide onboarding support, and develop strategic plans to support the team's RFP volume.
The Customer Success Manager will act as a primary point of contact to ensure successful customer onboarding, training, and ongoing service delivery. They will collaborate with internal teams like Sales, Applications, and R&D to remove barriers and drive positive business outcomes for clients.
You will support sales growth and customer success for advanced analytical and scientific instruments across diverse markets. This role involves developing strategic sales plans and building strong relationships with customers and internal stakeholders.
The Account Manager will drive revenue growth by developing strategic customer relationships and promoting a portfolio of scientific products. They will implement sales strategies, identify new business opportunities, and provide expert support to help customers achieve their goals.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of assigned studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
You will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Additionally, you will provide tailored scientific solutions to customers through consultative selling and cross-functional collaboration.
The Business Development Manager will identify and pursue strategic partnerships and commercial agreements within the biopharma sector to drive revenue growth. They will manage the full lifecycle of these partnerships, from initial negotiation and scoping to ongoing governance and performance tracking.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage documentation to ensure data reliability and subject safety.
The Sales Operations Analyst III will support sales incentive compensation deliverables, design compensation plans, and manage sales data quality. They will also lead special projects, coordinate territory mapping, and provide predictive insights using analytical tools.
The Field Application Scientist provides world-class technical support and expertise to customers, including product demonstrations, training, and troubleshooting. They work closely with sales teams to optimize technology usage and build long-term customer relationships.
The Regional Site Specialist will travel to various customer facilities to provide inventory, order, and chemical management support. They are also responsible for glass wash sterilization processes and driving process improvement initiatives.
The Project Manager provides tactical support for client-facing projects, managing financial performance and client communications throughout the clinical trial lifecycle. They also identify process improvement opportunities and escalate risks to project timelines and financial objectives.
The Global Regulatory Lead provides strategic and operational leadership for early-stage clinical programs, guiding them from first-in-human planning through proof of concept. They act as a key partner to cross-functional teams and health authorities to ensure high-quality regulatory submissions and development strategies.
The Safety Writer II is responsible for planning, coordinating, and delivering safety writing services for clinical trials and marketed products. This includes performing data reviews, authoring safety reports, and managing project communications within a regulated pharmacovigilance environment.
You will install, maintain, and repair a diverse range of high-value analytical instruments to ensure peak performance. Additionally, you will provide exceptional technical service and build strong relationships with customers to support their research and innovation.
Prepare and process financial transactions, manage billing and invoice operations, reconcile accounts, and support month-end activities using the Protheus ERP system and financial tools. Analyze financial data, maintain accurate records and internal controls, and collaborate across departments to ensure compliance with established procedures.
Coordinates clinical supply vendor services, including quotations, purchase orders, timelines, deliverables, and compliance with company procedures and client requirements. Reviews invoices and monitors purchase order balances and vendor costs, working with Procurement, Finance, Accounts Payable, and internal teams to resolve discrepancies and support timely payment.
Manage customer orders, inquiries, order status, back orders, and delivery confirmations while providing professional support through email and phone. Coordinate with internal teams and key accounts to resolve issues, meet service targets, improve processes, and maintain customer relationship records.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of projects regarding quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory requirements and internal SOPs.
The Sales Representative is responsible for promoting and driving revenue growth for Sanger Sequencing, qPCR, and digital PCR workflows within their assigned territory. They will collaborate with account managers and the sales force to execute strategic business plans and conduct scientific seminars.
Prepare, review, and coordinate country ethics committee and applicable Ministry of Health submissions in line with global strategy, while coordinating site start-up activities and timelines. Maintain trial tracking information and country study files, support informed consent and budget documentation, and follow applicable procedures and regulatory guidelines.
Perform day-to-day pharmacovigilance activities, including safety information intake and tracking, adverse event coding and assessment, case quality review, follow-up, and regulatory safety reporting. Coordinate project activities and collaborate with clients, investigators, reporters, and vendors; support meetings, audits, procedures, and the development of less experienced staff.
Conduct remote and on-site clinical monitoring visits, assess protocol and regulatory compliance, and manage required trial documentation. Ensure studies follow approved protocols, ICH-GCP, applicable regulations, and SOPs while maintaining audit readiness and collaborative relationships with investigational sites.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. Responsibilities include managing regulatory documents, tracking study metrics, and maintaining vendor trackers while ensuring compliance with SOPs and GCP guidelines.
Develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Collaborate with cross-functional teams to provide tailored scientific solutions and ensure high levels of customer satisfaction.
The Site Payments Associate is responsible for completing reconciliations of clinical trial payments in adherence to contractual guidelines and regulations. They will compile data from multiple sources, resolve payment-related issues, and manage relationships with study sites and teams.
The Site Payments Associate II provides administrative, reporting, and financial support for processing payments to investigative sites. They are responsible for compiling data, ensuring adherence to contractual and regulatory guidelines, and managing relationships with study sites.
The specialist will manage inventory using electronic systems and mobile scanning tools to ensure efficient order flow from dock to desk. They are responsible for performing cycle counts, replenishments, and maintaining accurate inventory records while providing excellent customer support.
Perform linguistic quality reviews of clinical and medical documents to ensure accuracy and regulatory compliance. Coordinate translation assets, manage terminology, and collaborate with global teams to improve translation quality processes.
The Manager of Clinical Operations oversees, trains, and mentors a team while ensuring adherence to SOPs and project performance metrics. They collaborate with leadership on resourcing, business development, and process improvement initiatives to ensure successful clinical trial delivery.
The Lead Account Manager will drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech clients. They will build executive-level relationships and manage strategic accounts to position the company as a preferred provider for life-changing therapies.
Lead and develop the North American SEM sales team and channel partners to grow bookings, pipeline, market coverage, and customer relationships. Provide market and competitive insights, manage sales performance and opportunity reviews, and collaborate across business teams to shape strategy and deliver a strong customer experience.
The Senior Project Manager acts as the primary client contact, overseeing the end-to-end delivery of clinical studies while managing budgets, timelines, and cross-functional teams. They are responsible for risk mitigation, stakeholder communication, and ensuring compliance with regulatory requirements and clinical standards.
Prepare and monitor Clinical Trial Agreements from initial site contact through execution, and review site budgets for forecasting and payment efficiency. Maintain communication between clinical teams and investigator sites, while providing technical and administrative support to Contract Analysts.
Install, maintain, and repair analytical instruments, including chromatography systems, and ensure they operate at peak performance. Provide technical service, troubleshoot complex issues, and build strong customer relationships while supporting scientific research and innovation.
Draft, review, negotiate, and finalize complex clinical trial contracts, ensuring regulatory and company-policy compliance and timely execution. Coordinate with internal teams and external stakeholders, maintain contract records, resolve contractual issues, and mentor junior specialists.
Develop new sales opportunities, advance existing opportunities to closure, and grow revenue and product adoption across the assigned territory. Partner with account managers and field application scientists on account strategies, sales planning, and technical solutions for complex customer needs.
Conduct remote or on-site monitoring visits to assess protocol and regulatory compliance, manage trial documentation, and ensure audit readiness. Coordinate site management and processes to ensure trials follow approved protocols, ICH-GCP guidelines, applicable regulations, and SOPs while protecting participants and supporting reliable data.
The Vendor Management Coordinator supports clinical supply operations by managing vendor relationships, processing purchase orders, and ensuring invoice accuracy. They also coordinate with cross-functional teams to ensure study requirements, timelines, and quality standards are met.
Drive market development and demand generation for the clinical NGS portfolio by translating regional strategies into local initiatives. Collaborate closely with sales teams and clinical stakeholders to accelerate customer engagement and technology adoption.
The manager is responsible for overseeing site monitoring strategies, conducting risk assessments, and ensuring trial quality through trend analysis and signal detection. They lead cross-functional teams to maintain regulatory compliance, patient safety, and data integrity across clinical trials.
The Country Approval Specialist supports study startup by managing and coordinating local regulatory submissions in alignment with global strategies. They act as a key contact for regulatory activities and ensure site start-up processes are aligned with critical project timelines.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions to ensure alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities while overseeing site start-up activities and ensuring compliance with SOPs.
Drive sales growth and manage key accounts across academic, government, and industrial sectors within the Illinois territory. Execute effective sales strategies, maintain a robust sales pipeline, and deliver technical solutions to meet or exceed revenue targets.
The Field Applications Scientist will serve as a subject matter expert in protein expression workflows, providing pre- and post-sales scientific support and training to customers. This role involves troubleshooting complex technical challenges and partnering with internal teams to optimize protein production and downstream workflows.
The Regulatory Affairs Manager will own regulatory decision-making for clinical programs and drive cross-functional teams to execute regulatory strategies. They are responsible for providing strategic guidance, managing regulatory submissions, and ensuring compliance throughout the product development lifecycle.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Manages site processes, escalates issues for resolution, and maintains documentation throughout the clinical trial lifecycle.
The Senior Clinical Trial Manager leads local study teams to ensure clinical studies are delivered on time, within budget, and in compliance with international and local regulations. They are responsible for site selection, monitoring activities, financial management, and maintaining high-quality data throughout the study lifecycle.
The Trial Strategy Specialist III provides expert guidance in the formulation and execution of clinical trial strategies to ensure operational success. They collaborate with cross-functional teams to develop operational models, manage budgets, and ensure alignment with commercial win strategies.
The Medical Director provides medical leadership and support for clinical trials, including protocol creation, site selection, and real-time medical monitoring. They serve as the primary medical point of contact for internal and external stakeholders, ensuring study compliance and safety throughout all phases.
The Senior Sales Manager will lead a sales team to drive strategic growth and manage customer relationships within the East Subregion. Responsibilities include developing sales strategies, maintaining a strong pipeline, and ensuring the team meets revenue targets.
The Local Study Associate Director leads local study teams to ensure clinical studies are delivered on time, within budget, and in compliance with international guidelines and local regulations. They oversee site selection, monitoring activities, financial management, and regulatory submissions throughout the study lifecycle.
Provide medical leadership to study teams by creating protocols, ensuring subject safety, and performing real-time medical monitoring. Collaborate with cross-functional teams to interpret clinical data and ensure compliance with regulatory standards and SOPs.
The Principal Clinical Trial Coordinator oversees and facilitates project activities, acting as a cross-functional liaison to ensure clinical trial execution excellence. They are responsible for managing site activation, maintaining study documentation, and ensuring compliance with regulatory standards and internal SOPs.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, maintain databases, and collaborate with sites to ensure compliance with regulatory guidelines and SOPs.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring site activation activities and trial documentation meet quality standards. They manage site files, reconcile study metrics, and facilitate communication between internal teams and clinical sites to ensure audit readiness.
The Principal Clinical Trial Coordinator oversees administrative and technical project activities, acting as a cross-functional liaison to ensure study execution excellence. They are responsible for site activation, regulatory document management, and providing training to staff while maintaining compliance with global standards.
The Site Payment Associate II is responsible for end-to-end site payment management, including generating payment requests and tracking invoice data in Veeva Clinical. They also collaborate with clinical trial managers to set up fee schedules and ensure payments align with study milestones and contractual guidelines.
The VP of Medical Science and Strategy will lead the development and execution of medical strategies for cardiovascular programs. This role involves cross-functional leadership to ensure scientific excellence and alignment with clinical development goals.
The Site Payment Associate II is responsible for end-to-end site payment management, including generating payment requests and managing invoice data in Veeva Clinical. They also provide administrative, reporting, and financial support while ensuring adherence to contractual guidelines and country regulations.
The specialist will coordinate and manage the quality of clinical translations, including protocols and patient documentation. They will also maintain terminology assets and execute linguistic quality assurance processes globally.
The Senior Programmer Analyst leads bioinformatics programming activities and manages clinical trial data projects independently. They are responsible for creating and validating programs, mentoring junior staff, and collaborating with multi-disciplinary teams to meet project timelines.
The IT Director is responsible for defining and executing the global technology strategy for the Finance function within the Clinical Trials Division. This role leads finance system transformation, ERP modernization, and the standardization of global business processes to drive operational excellence.
Lead and develop a team of four field-based application scientists while providing hands-on technical support for transplant diagnostics solutions. Coordinate field activities, prioritize customer needs, and ensure technical excellence across the DACH region and broader EMEA territory.
You will serve as a technical expert providing comprehensive support for analytical instrumentation and building strong relationships with customers and internal partners. The role involves delivering technical training, optimizing applications, troubleshooting complex issues, and contributing to product development through customer feedback.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, maintain databases, and coordinate with internal and external stakeholders to meet project timelines.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also serve as the primary contact for regulatory activities and ensure site start-up processes meet established timelines.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategy. They serve as a primary contact for investigators and regulatory authorities to ensure timely site activation and compliance.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions to ensure alignment with global strategies. They serve as the primary contact for investigators and regulatory authorities while overseeing site start-up activities and maintaining compliance with SOPs.
Develop and implement global business development strategies for Oncology companion diagnostics to drive growth and market penetration. Coordinate the full deal lifecycle, including lead generation, proposal development, and contract negotiations while collaborating with cross-functional teams.
The Account Development Specialist is responsible for re-engaging and growing a portfolio of underpenetrated customer accounts through virtual selling channels. They will proactively prospect, manage a defined book of business, and partner with Inside Sales Representatives to drive revenue growth.
The Associate Director ensures the delivery of safety management services in compliance with regulatory requirements and company SOPs. They oversee departmental operations, manage staff, and support business development by fostering client relationships and providing operational input on proposals.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory requirements and internal SOPs.
The Strategic Account Manager will drive reagent revenue growth and customer retention across a portfolio of laboratories and health systems. They will develop strategic account plans and serve as the primary commercial partner for key stakeholders to optimize laboratory efficiency and patient outcomes.
Performs and coordinates all aspects of the clinical monitoring and site management process to ensure protocol and regulatory compliance. Conducts on-site and remote monitoring visits to assess data accuracy, site processes, and audit readiness.
The Sr CM Analyst II will identify and characterize issues and trends in clinical trial data using analytical tools to inform project teams. Key duties include conducting risk assessments, developing monitoring plans, ensuring regulatory compliance, and maintaining inspection readiness.
The Country Study Manager leads the operational implementation, planning, and delivery of clinical studies within the country to ensure high-quality execution per protocol and budget. They serve as the primary operational contact between the Central Study Team and local staff, managing site selection, vendor oversight, and regulatory submissions.
The Field Application Specialist will manage the installation, configuration, and training for clinical laboratory products, ensuring seamless integration with Laboratory Information Systems. They will also provide ongoing technical support, resolve customer complaints, and maintain accurate service records while traveling to various clinical sites.
Drive sales growth and customer success across the Product Inspection portfolio by recommending instrumentation and software solutions. Build and maintain strong customer relationships while managing a sales pipeline to achieve targets within food, pharmaceutical, and manufacturing sectors.
You will develop and execute integrated marketing campaigns and sales enablement tools to support the Pharma/BioPharma portfolio. The role involves collaborating with cross-functional teams to translate technical capabilities into clear value propositions that drive market growth.
The role involves acting as a subject matter expert to develop tools and processes for detecting and mitigating clinical trial risks. You will lead centralized monitoring activities, perform complex data reviews, and coordinate with cross-functional teams to ensure trial quality and patient safety.
Acts as a subject matter expert to develop tools and processes for detecting and mitigating clinical trial risks. Leads centralized monitoring activities, manages project deliverables, and coordinates with cross-functional teams to ensure data integrity and patient safety.
The Senior Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, regulatory compliance, and protocol adherence. They also mentor team members, facilitate communication between sites and the project team, and contribute to process improvements.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform site visits, manage documentation, and ensure data reliability while maintaining collaborative relationships with investigational sites.
The Senior Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They also facilitate communication between investigative sites, clients, and the project team while mentoring new staff and contributing to project documentation.
The Senior Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They also facilitate communication between investigative sites and the project team while mentoring new staff and contributing to project documentation.
The Regional Product Manager drives the commercial success, growth, and lifecycle management of the protein diagnostics portfolio across North America. This role leads cross-functional initiatives to align global strategy with regional market needs while managing product launches and customer engagement.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage documentation to ensure data reliability and subject safety.
The Sr CM Analyst II will identify and characterize issues and trends in clinical trial data using analytical tools to support operational excellence. They are responsible for conducting risk assessments, developing monitoring plans, and ensuring regulatory compliance and inspection readiness.
The Field Service Engineer is responsible for the installation, repair, and preventative maintenance of chromatography and mass spectrometry equipment. They must manage customer relationships, ensure service level agreement compliance, and provide technical training to clients.
The Field Service Engineer will perform repairs, installations, and preventative maintenance on various laboratory equipment at customer sites. They are responsible for managing spare parts inventory, documenting service actions, and maintaining strong customer relationships.
The Technical Sales Specialist will drive revenue growth and customer success by providing technical expertise for a portfolio of scientific instruments and solutions. They will manage key accounts, develop sales strategies, and collaborate with cross-functional teams to deliver effective solutions for biotechnology and pharmaceutical customers.
Provide pre-sales and post-sales scientific support, training, and workflow guidance for cell therapy instrumentation. Collaborate with commercial teams to build customer relationships and represent the company at scientific events.
You will perform and coordinate all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. You will act as a dedicated representative for the client, managing site processes and maintaining strong relationships with investigational sites.
Lead commercial strategy and business development for global pharmaceutical accounts, developing account plans and closing large, multi-year opportunities for proteomics and biomarker discovery solutions. Coordinate across sales, scientific, product, and global teams; engage senior customer leaders; and coach field teams to strengthen strategic customer interactions.
Lead a team of strategic account managers and deliver revenue and bookings for a portfolio of major semiconductor accounts, including responsibility for more than $100 million in annual business. Develop global account strategies, build executive customer relationships, manage pipeline and commercial negotiations, coordinate internal teams, and provide forecasts and performance updates.
Coordinate and oversee clinical trial activities, documentation, regulatory submissions, feasibility work, and site activation, ensuring tasks are accurate, timely, and aligned with project requirements. Serve as a cross-functional and client liaison, support audit readiness and process improvements, and train colleagues while escalating project risks as needed.
Install, maintain, troubleshoot, and repair sophisticated analytical and scientific instruments for customers in research, industrial, and healthcare settings. Provide responsive customer support, train customers on equipment operation, and document service activities in detailed reports.
The Field Service Engineer will install, maintain, and repair sophisticated analytical instruments to ensure peak performance. They will act as a company representative, providing exceptional technical service and building strong relationships with customers.
The Regulatory Affairs Specialist provides operational and administrative support for Chemistry, Manufacturing and Controls (CMC) documentation to ensure inspection-ready regulatory submissions. This role coordinates submission content, maintains regulatory records, and collaborates with internal and external partners to ensure compliance with global requirements.
The Associate Safety Reporting Specialist manages the receipt, submission, and tracking of safety reports while ensuring compliance with regulatory timelines. They also support project management tasks, maintain safety databases, and assist in the preparation of regulatory submission files.
The Principal Clinical Trial Coordinator oversees and facilitates project activities, acting as a cross-functional liaison to ensure clinical trials are executed on time and within budget. They provide administrative and technical support, manage site activation paths, and serve as a subject matter expert for process improvements and team training.
The Principal Clinical Trial Coordinator oversees and facilitates project activities, acting as a cross-functional liaison to ensure clinical trial execution excellence. They manage site activation, maintain study documentation, and provide technical support to project teams while ensuring adherence to regulatory and quality standards.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The Product Specialist is responsible for driving revenue growth and market share for laboratory chemicals across Queensland, New South Wales, and New Zealand. They will manage the end-to-end sales process, develop territory strategies, and provide technical solutions to meet customer needs.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and sponsors.
The Account Executive is responsible for selling diagnostic lab supplies and instrumentation while maintaining effective customer relations within a defined territory. They must develop sales strategies, manage a pipeline of opportunities, and ensure market penetration and profitability.
You will lead a sales team to drive business growth and customer success across research, clinical, and commercial production markets. This involves developing strategic sales plans, analyzing market trends, and ensuring the team meets or exceeds profitability targets.
Monitor and manage clinical trial sites through remote and on-site visits, ensuring protocol, regulatory, and ICH-GCP compliance, reliable data, complete documentation, and audit readiness. Communicate with sites, sponsors, and project teams; resolve findings, track study progress, and support trial initiation, conduct, and closeout.
The Safety Reporting Specialist manages and coordinates the production of regulatory and safety reports while ensuring compliance with global pharmacovigilance requirements. They also participate in project teams, provide training to team members, and maintain safety reporting systems.
Provide comprehensive pre-sales and post-sales technical support, including product demonstrations, hands-on training, and troubleshooting for qPCR technologies. Collaborate with sales and cross-functional teams to build long-term customer relationships and support business objectives.
The Associate Director will lead core financial rhythms including AOP, forecast cycles, and month-end close while providing financial planning support across the Analytical Services Division. They will partner with cross-functional stakeholders to translate complex financial data into clear business insights and executive-ready deliverables.
The Start-up Team Manager oversees complex site operations, ensuring compliance with regulatory standards and managing site activation timelines. They facilitate collaboration between internal teams and clinical sites while managing financial and contractual aspects of the studies.
The role involves leading portfolio growth for Biotech customers through strategic governance, planning, and cross-functional collaboration across Pharma and Clinical Research groups. The leader will manage customer relationships, oversee project teams, and facilitate risk mitigation to ensure seamless service delivery.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
The Comparator Sourcing Lead will manage market intelligence and sourcing strategies for clinical trial supplies to support client portfolio requirements. This role involves executing purchase orders, overseeing delivery, and acting as a subject matter expert on external market trends and regulatory landscapes.
The Manager of Site Payments will lead a team to ensure accurate and compliant investigator payments while driving operational excellence across clinical trials. They are responsible for managing project delivery, mentoring staff, and implementing process improvements to support the FSP Business Unit.
The HGRAC CAS is responsible for managing all HGRAC applications for clinical operation studies in China and supporting human genetic resource management during trial implementation. This role involves preparing and reviewing application documents, tracking status, and providing regulatory guidance to internal delivery teams.
The specialist is responsible for managing all HGRAC applications for clinical studies in China and ensuring compliance with regulatory requirements. They also maintain databases for regulations and provide strategic support to internal delivery teams regarding HGRAC processes.
The Senior Business Development Manager is responsible for driving sales growth and acquiring new customers within the Cell & Gene Therapy sector. They will develop territory strategies, build executive relationships, and position integrated supply chain solutions to support customer development programs.
You will coordinate all aspects of clinical monitoring and site management to ensure protocol compliance and data accuracy. This involves conducting remote or on-site visits, managing documentation, and acting as a primary liaison between the client and investigative sites.
The Project Manager leads and coordinates central laboratory activities across clinical trial programs to ensure project performance and client satisfaction. They act as the primary liaison between sponsors and internal departments while maintaining study documentation and ensuring regulatory compliance.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
The Field Service Engineer will perform on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and maintain detailed service reports while acting as a subject matter expert.
Conduct impartial investigations into internal complaints and potential policy or Code of Conduct violations, coordinating interviews and maintaining accurate records. Prepare reports with findings, recommendations, and root cause analysis, and partner with ER, legal, and HR colleagues to strengthen ethical culture programs.
Manage full-cycle recruitment across manufacturing, operations, commercial, research and development, and corporate functions, partnering with hiring managers to attract and secure qualified candidates. Develop sourcing strategies, conduct competency-based interviews, build stakeholder relationships, provide an excellent candidate experience, and ensure compliance with employment laws and company policies.
The Principal Regulatory Affairs Specialist provides strategic regulatory guidance and intelligence to support product development from preclinical stages through registration. They also lead project teams, ensure compliance with global regulatory requirements, and manage client deliverables and budgets.
The Principal Regulatory Affairs Specialist will lead regulatory strategies and manage submissions to ANVISA for clinical trials in Brazil. They will act as a local expert, interacting with sponsors, internal teams, and regulatory authorities to ensure compliance and project success.
The manager will oversee, coach, and mentor a team of clinical operations staff while ensuring adherence to company SOPs and performance metrics. They will also collaborate with leadership on resourcing, business development, and process improvement initiatives.
The Compliance Manager will provide clinical quality oversight and serve as a single point of contact for client partners to establish a consistent quality culture. They will facilitate quality risk management, analyze quality metrics, and drive support for partnership governance and joint quality councils.
Manage the end-to-end supply chain for clinical trials to ensure timely distribution of materials and optimal inventory levels. Collaborate with cross-functional teams to integrate supply chain activities and ensure compliance with GxP requirements.
Lead the development of project timelines, budgets, and forecasts while ensuring the quality and compliance of Informed Consent Forms. Collaborate with cross-functional teams to monitor project status and resolve client management issues.
Lead a team of marketing professionals to develop and execute growth strategies that drive customer adoption and business impact. Partner with cross-functional teams including product management and sales to translate market insights into effective commercialization programs.
The Associate Manager Clinical Operations oversees daily line management, performance, and professional development for a team of clinical operations personnel. They collaborate with senior management on strategic planning while ensuring adherence to SOPs and optimizing project resourcing.
The Senior Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of clinical study sites to ensure compliance with international guidelines and company procedures. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring visits and risk assessments.
The Contract Manager leads the preparation, negotiation, and finalization of contract templates and investigator grant budgets while ensuring quality and risk mitigation. They also serve as a regional lead, providing oversight, training, and mentoring to team members while acting as a primary interface for external clients.
The Associate Contract Manager leads the review, negotiation, and finalization of contract templates and investigator grant budgets while providing regional oversight. They also act as a primary interface for clients and provide training and mentorship to team members.
Leads patient-centric medical writing projects with a focus on Informed Consent Forms while managing timelines, budgets, and resources. Collaborates with cross-functional teams and clients to ensure high-quality deliverables and effective project management.
The Senior Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of complex, cross-functional projects in terms of quality, time, and cost. They are responsible for driving risk identification, managing financial stewardship, and ensuring team compliance with regulatory and organizational standards.
Lead country-level Local Study Teams and oversee clinical study delivery, including site selection, activation, monitoring, recruitment, budgets, regulatory submissions, and compliance with ICH-GCP and local requirements. Manage study risks, documentation, team performance, stakeholder communications, and readiness for audits, inspections, and final archiving.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of cross-functional projects regarding quality, time, and cost. They are responsible for managing customer expectations, driving risk identification, and ensuring team compliance with regulatory and organizational standards.
The Senior Project Manager acts as the primary sponsor contact and is accountable for the overall delivery of complex projects in terms of quality, time, and cost. They lead cross-functional teams, manage financial budgets, and ensure compliance with regulatory and organizational standards.
Serve as a bioprocessing domain expert to support customers with technology adoption, process design, and optimization across downstream workflows. Lead technical activities including product evaluations, troubleshooting, and training while gathering customer feedback to inform product development.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and closure of clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, driving performance and ensuring timely resolution of study-related issues.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
Develop and execute strategic sales plans to drive revenue growth and expand market penetration within assigned global key accounts. Build and maintain strong relationships with senior-level clients while leading the RFP and RFI processes to secure preferred provider opportunities.
You will coordinate all aspects of clinical monitoring and site management to ensure trial protocol and regulatory compliance. This involves conducting remote or on-site visits, managing documentation, and ensuring data reliability in accordance with ICH-GCP guidelines.
The Country Approval Specialist manages, reviews, and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet project timelines.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including document collection, system access, and remote monitoring tasks. They assist in coordinating study start-up, recruitment, and close-out phases while ensuring compliance with SOPs and regulatory guidelines.
The Start-up Team Manager oversees complex site operations, ensuring regulatory compliance and effective site activation for clinical studies. They facilitate communication between internal teams and clients while managing project budgets, timelines, and risk mitigation strategies.
The FSP Manager is responsible for the line and functional management of employees dedicated to a specific client under an FSP model. This includes recruiting, onboarding, mentoring staff, and ensuring performance metrics are met while acting as the primary point of escalation.
Provide expert installation, maintenance, and repair services for HPLC and Mass Spectrometry instrumentation. Manage company assets, resolve technical issues, and deliver outstanding technical support to customers across research and industrial facilities.
The Digital Support Engineer will manage IT infrastructure integration for digital solutions and provide remote support for customer deployments. They will also conduct troubleshooting and analysis to ensure system reliability and performance.
The Clinical Trial Coordinator provides administrative and technical support for clinical trials, including site activation, file reviews, and regulatory document management. They ensure trial activities are performed on time and within budget while maintaining compliance with SOPs and regulatory guidelines.
The Clinical Research Associate coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site processes, manage documentation, and ensure audit readiness.
The Manager Clinical Operations oversees, trains, and mentors a team while ensuring adherence to company SOPs and regulatory standards. They manage performance metrics, resource allocation, and collaborate with leadership to drive process improvements and business development.
The Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage site relationships, and support the clinical team in delivering quality research outcomes.
The Enterprise Market Development Manager identifies and advances strategic growth opportunities across health systems and integrated healthcare networks. This role builds relationships with executive stakeholders and coordinates cross-functional resources to convert enterprise opportunities into actionable commercial initiatives.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol and regulatory compliance. You will conduct remote or on-site visits to assess data accuracy, manage documentation, and resolve site-related issues.
The Senior Manager, Sales is responsible for achieving quarterly and annual sales targets for Chromatography and Mass Spectrometry product lines within their territory. They will lead, coach, and develop a team of sales representatives while collaborating with internal business units to drive market share growth and customer loyalty.
The Senior Manager, Sales is responsible for achieving quarterly and annual sales targets for Chromatography and Mass Spectrometry product lines within their territory. They will lead, coach, and develop a team of sales representatives while collaborating with internal business units to drive market share growth and customer satisfaction.
Lead, mentor, and develop a team of field service engineers while coordinating daily service operations and ensuring timely issue resolution. Manage service KPIs, maintain strong customer relationships, and ensure compliance with safety and regulatory standards.
The Sr Biostatistician II functions as a lead statistician to deliver analysis databases, statistical analyses, and formatted reports for clinical research projects. They also provide mentorship to junior team members and collaborate with sponsors and regulatory agencies.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing complex analytical and scientific instruments. They must provide exceptional customer service while documenting service activities and training customers on equipment operation.
Manage all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. Coordinate clinical team activities, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
Provide expert installation, maintenance, and repair services for sophisticated analytical and microscopy equipment. Build strong customer relationships while resolving complex technical issues and training users on system performance.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
The role involves leading safety data management and system maintenance activities while ensuring high-quality data outputs for signal and risk management. The associate manager will also collaborate with cross-functional teams and vendors to support compliant drug safety case processing and system administration.
Lead and coach the regional talent acquisition team, partnering with business leaders and HR teams to develop hiring strategies and plans aligned with business needs. Manage end-to-end recruitment, improve processes and technology adoption, and ensure a positive candidate experience and timely hiring outcomes.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol and regulatory compliance. You will conduct remote or on-site visits, manage site documentation, and mentor junior team members to ensure data reliability and subject well-being.
The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate effective communication between investigative sites and the project team.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, driving performance, managing study supplies, and ensuring data quality through regular monitoring visits and site quality assessments.
The Clinical Research Associate is responsible for monitoring clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, managing site initiation, performance, data quality, and regulatory documentation throughout the study lifecycle.
The Technical Sales Specialist will drive sales for GeneArt gene synthesis and cloning services by consulting with researchers to provide comprehensive molecular biology workflow solutions. This role involves building scientific relationships, managing territory business plans, and collaborating with internal teams to identify and capture new business opportunities.
Install, maintain, troubleshoot, and repair chromatography and mass spectrometry equipment at customer laboratories, while documenting service work and managing parts inventory. Train customers, communicate service needs across internal teams, and use customer data and factory protocols to diagnose and expedite complex repairs.
Leads and develops clinical operations staff, overseeing onboarding, training, resourcing, performance management, and professional development. Monitors project and employee metrics, supports quality and audit activities, escalates delivery risks, and collaborates with leadership on operational planning and improvement.
Lead planning, monitoring, and delivery of CMC development projects, managing timelines, budgets, scope, risks, dependencies, and stakeholder coordination. Provide regulatory strategy and submission guidance, oversee project quality and compliance, and support client relationships, business development, and junior team members.
The specialist will design and improve products and processes to optimize operational performance and ensure audit readiness. They will lead process improvement initiatives and collaborate with cross-functional teams to support clinical research outcomes.
The Medical Project Coordinator will support drug safety operations by reviewing safety data, identifying trends, and ensuring compliance with regulatory standards. They will also manage project implementation, coordinate with stakeholders, and assist in the creation of safety management plans.
The recruiter will manage full-cycle recruitment for diverse roles while serving as a strategic talent advisor to hiring managers. They will develop effective sourcing strategies, build talent pipelines, and ensure a positive candidate experience.
Draft, review, negotiate, and finalize clinical study site agreements and investigator grant budgets within approved parameters and established processes. Assess and escalate contractual, financial, and operational risks while coordinating site startup activities and timelines to support efficient site activation.
The Senior Safety Specialist will perform and oversee day-to-day Pharmacovigilance activities, including the collection, monitoring, and evaluation of safety information. They will also coordinate project implementation, mentor junior staff, and ensure compliance with global regulatory requirements.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
The Site Payments Associate is responsible for processing investigator payments in strict adherence to contractual guidelines and country regulations. They also manage site study budgets and resolve payment-related issues to ensure accurate financial operations.
The Senior Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They are responsible for documenting observations, managing site issues, and coordinating with project teams to ensure successful clinical trial execution.
You will negotiate and manage complex federal and commercial agreements while collaborating with cross-functional teams to ensure compliance and business growth. Additionally, you will serve as a trusted advisor on contracting matters, developing strategies to mitigate risk and protect company interests.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage corrective actions for site process failures.
The role leads global sales strategy development and execution to drive revenue growth within the downstream bioprocessing business. It involves coordinating commercial efforts across various internal functions and managing a global sales team to meet strategic objectives.
The Medical Writer is responsible for producing high-quality medical and scientific documentation, including clinical study documents and medical information. They collaborate with internal and external clients to ensure operational excellence while maintaining compliance with SOPs and quality standards.
Provide technical and application support for electrochemistry products to end users and channel partners via phone and email. Collaborate with internal teams including Marketing, R&D, and Quality to resolve product issues and contribute to continuous improvement initiatives.
The Assistant CRA performs remote site management and monitoring activities to ensure clinical trial compliance with regulations and protocols. They maintain communication with site staff, resolve data queries, and track study progress using various clinical systems.
The Associate Manager oversees the daily line management, coaching, and professional development of clinical administration staff. They also collaborate with senior management on strategic planning, resourcing, and ensuring adherence to SOPs and performance metrics.
Act as a technical advisor for bioprocessing hardware and automation, supporting customers with process development, scale-up, and troubleshooting. Lead technical activities including workflow assessments, technology qualification, and training to ensure successful adoption of bioproduction solutions.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage site-level issues through root cause analysis and corrective actions.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Manages site relationships, conducts remote or on-site visits, and ensures audit readiness in accordance with ICH-GCP guidelines.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Conducts remote or on-site visits to assess regulatory adherence and manages corrective actions to mitigate risks.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Conducts remote or on-site visits to assess regulatory adherence and manages corrective actions to mitigate risks.
Performs and coordinates clinical monitoring and site management processes to ensure protocol and regulatory compliance. Manages site relationships, conducts data reviews, and ensures audit readiness throughout the clinical trial lifecycle.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol compliance and data reliability. You will conduct remote or on-site visits, manage site documentation, and mentor junior team members while maintaining collaborative relationships with investigational sites.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol compliance and data reliability. You will conduct remote or on-site visits, manage documentation, and mentor junior team members to support clinical trial objectives.
The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-level issues.
The Senior Director leads a national team of Health Systems Executive Directors to drive sales strategy and market share growth within key healthcare accounts. They are responsible for building executive-level relationships, managing large enterprise partnerships, and overseeing the implementation of complex contracts.
The Proposal Specialist develops high-quality, technically sound proposals, scopes, and Statements of Work for mRNA and lipid nanoparticle programs. They collaborate with cross-functional teams to define project resources, pricing, and timelines while acting as a primary liaison between clients and technical subject matter experts.
Manage the end-to-end supply chain for clinical trials to ensure timely distribution of materials and maintain optimal inventory levels. Collaborate with cross-functional teams to integrate supply chain activities while ensuring compliance with GxP requirements.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
The incumbent will serve as a subject matter expert in oncology to support business development, proposal strategy, and bid defenses. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and oversee the design of clinical trial protocols and regulatory documentation.
The role involves driving operational excellence in clinical study management by collaborating with internal and external partners to ensure data integrity and inspection readiness. Responsibilities include managing study-related activities, overseeing vendors and CROs, and monitoring study progress against quality, timeline, and budget objectives.
You will draft, review, and negotiate clinical trial site agreements while ensuring compliance with budgetary and contractual parameters. Additionally, you will coordinate with internal teams to manage site startup activities and mitigate legal, financial, and operational risks.
Lead business delivery and readiness for the end-to-end Oracle Financials implementation, including requirements, testing, data migration, training, cutover, go-live, and stabilization. Coordinate stakeholders across Finance, IT, business teams, and implementation partners while managing risks, issues, dependencies, and delivery reporting.
The Clinical Trial Coordinator will provide administrative and technical support to project teams while facilitating project activities and serving as a cross-functional liaison. Responsibilities include managing study documentation, performing file reviews, ensuring compliance with regulatory standards, and supporting system-specific tasks.
The Principal Site Payment Associate leads administrative, financial, and contractual support for processing payments to FSP investigative sites. Responsibilities include reviewing budgets, managing reconciliations, ensuring regulatory compliance, and mentoring junior team members.
The Country Approval Specialist coordinates and prepares local regulatory submissions for clinical trials in alignment with global strategies. They also serve as a key point of contact for regulatory activities and ensure site start-up processes meet established timelines.
The Associate Site Contract Specialist drafts, reviews, and negotiates clinical trial site contracts and budgets while ensuring compliance with internal and client processes. They coordinate with internal functional teams to align site startup activities with contractual timelines and target cycle times.
The Manager Clinical Operations oversees, trains, and mentors a team of clinical staff while ensuring adherence to company SOPs and regulatory standards. They are responsible for managing performance metrics, resourcing, and collaborating with leadership on strategic planning and business development.
The Director of Strategic Accounts leads a team of Strategic Account Leaders to drive growth, profitability, and customer experience across a portfolio of biopharma accounts. They are responsible for setting enterprise account strategies, fostering senior-level client relationships, and ensuring cross-divisional alignment to meet commercial objectives.
The Senior Clinical Research Associate will coordinate all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They will also provide mentorship to junior team members and collaborate with cross-functional teams to implement study plans effectively.
The Executive Account Director will develop and execute strategic sales plans to drive growth and maximize business opportunities within assigned global key accounts. They will lead RFP processes, manage client relationships, and collaborate with internal teams to ensure customer satisfaction and preferred vendor status.
The Clinical Trial Coordinator assists in the administration and coordination of clinical studies from start-up through execution to close-out. They ensure document quality, maintain regulatory compliance, and serve as the primary administrative contact for the study team.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs and availability for clinical research projects. They also liaise with internal departments to prioritize staffing and ensure project teams are optimized for quality and financial performance.
The Pharmacovigilance Physician provides medical oversight for pharmacovigilance activities, ensuring compliance with regulatory requirements and company SOPs. They are responsible for the medical review of serious adverse events, signal detection, and the preparation of periodic safety reports.
The Technical Sales Specialist will drive revenue growth by managing a portfolio of chemical analysis instruments and developing territory sales plans. They will build strong customer relationships, provide technical expertise, and collaborate with internal teams to ensure customer success and market expansion.
The Field Applications Scientist will serve as a technical advisor, providing pre-sales and post-sales support through product demonstrations, training, and troubleshooting. They will collaborate with sales teams to help customers optimize advanced technologies and achieve scientific discoveries.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage essential documentation, and facilitate communication between investigative sites and sponsors.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence using a risk-based approach. They will also facilitate communication between sites, sponsors, and the project team while managing essential documentation and trial progress.
The SR CRA II coordinates clinical monitoring and site management processes to ensure trials comply with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage documentation to ensure data reliability and audit readiness.
Coordinate all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. Conduct on-site and remote visits to assess regulatory adherence and manage corrective actions for site process failures.
Design and validate AI/ML and NLP components to support safety operations, including auto-coding, case triage, and narrative summarization. Serve as the primary technical resource for the configuration, maintenance, and administration of the Oracle Argus Safety system.
The Director of Business Development will build Olink’s presence in the protein diagnostics market by developing strategic partnerships and customer relationships. They will identify new business opportunities and translate market needs into actionable commercial plans to drive revenue growth.
You will install, maintain, and repair complex Dualbeam electron microscopy systems at customer sites, including semiconductor fabrication facilities. You will also serve as a technical partner by diagnosing issues, performing preventive maintenance, and training customers on equipment operation.
The Product Sales Specialist will provide technical guidance and promote the company's life sciences product portfolio to academic, pharmaceutical, and industrial customers. They are responsible for conducting product demonstrations, managing customer relationships, and delivering effective value propositions to drive sales growth.
Install, maintain, troubleshoot, and repair advanced analytical instrumentation such as OES, XRF, and XRD systems at customer sites. Manage service calls, parts inventory, and provide technical training to customers and colleagues.
The Principal Regulatory Affairs Assistant provides advanced administrative and operational support to the regulatory affairs department, including project coordination and documentation management. They are responsible for compiling submissions, tracking deliverables, and ensuring compliance with internal and sponsor standard operating procedures.
The Strategic Key Account Manager will develop and maintain high-value relationships with key customers to drive business growth and success. They will coordinate cross-functional teams to deliver integrated solutions and execute complex, multi-year commercial agreements.
Develop business by selling clinical research and laboratory services to pharmaceutical and biotechnology clients, including bioanalytical and biomarker services. Lead RFP strategy, proposals, presentations, negotiations, and contract closures while managing client relationships, satisfaction, sales activity, and new business authorizations.
Lead scientific work across research projects and author, review, and finalize client deliverables such as protocols, reports, analysis plans, evidence dossiers, presentations, and manuscripts. Manage project scope, timelines, budgets, and staffing; engage with clients; mentor junior staff; and contribute to proposals, conferences, training, recruitment, and regulatory meeting preparation.
Lead clinical staff and managers across multiple countries or a geographic area to deliver clinical studies on time, within quality standards, and within budget. Oversee staffing, project strategy, financial performance, risk escalation, training, compliance, and collaboration with cross-functional teams and clients.
Lead and oversee a portfolio of research projects, ensuring scientific quality, timely delivery, and adherence to contracted budgets while presenting findings in peer-reviewed journals and at professional meetings. Provide scientific leadership and mentorship to junior staff, delegate project tasks, and develop client relationships and business opportunities.
Provide installation, repair, maintenance, validation, and other field service support for trace elemental analytical instruments, primarily ICP-OES and ICP-MS, across the North West of England and potentially elsewhere. Deliver high-quality customer support, coordinate service activities and resources, manage company equipment and inventory, and submit accurate service and expense reports.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They oversee clinical monitoring processes, maintain trial documentation, and collaborate with cross-functional teams to ensure study compliance and project success.
Conduct clinical research monitoring while applying clinical monitoring skills and relevant medical and therapeutic area knowledge. Use risk-based monitoring concepts and processes, investigate issues through root cause analysis, and communicate effectively with medical personnel and customers.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, perform file reviews, and maintain study metrics to ensure compliance with regulatory guidelines and SOPs.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, perform file reviews, and maintain communication with clinical sites to ensure project timelines and quality standards are met.
Provide technical expertise and application engineering support for industrial filtration and separation solutions across Latin America. Drive growth by collaborating with customers, industry experts, and cross-functional teams to implement purification solutions and maximize technology value.
The Clinical Trial Coordinator II provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and oversee regulatory compliance across clinical trials.
Manage assigned clinical study sites from preparation and initiation through monitoring and closure, ensuring compliance with company procedures, ICH-GCP, and local regulations. Monitor site performance and data quality, support investigators and site staff, maintain study documentation and supplies, and promptly resolve or escalate study-related issues.
Leads, coaches, trains, and performance-manages clinical operations staff, while supporting recruitment, onboarding, career development, and resource allocation. Monitors project and employee performance using metrics and systems, promotes regulatory and quality compliance, supports audits and risk-based monitoring, and contributes to process improvement and business initiatives.
Monitor clinical trial sites using risk-based methods, verify data and investigational product records, and document and escalate findings through resolution. Support site selection, initiation, ongoing compliance, closeout, essential document reviews, investigator payments, and study status reporting.
The Associate Manager Clinical Operations oversees daily line management, coaching, and professional development for clinical operations staff. They collaborate with senior management on strategic planning, resourcing, and ensuring adherence to company SOPs and quality standards.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage site-level issues through risk-based monitoring.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate effective communication between investigative sites and the project team.
The Clinical Research Associate is responsible for monitoring clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, managing site initiation, performance, data quality, and regulatory documentation throughout the study lifecycle.
The Country Approval Specialist manages, reviews, and coordinates local regulatory submissions in alignment with global submission strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet established timelines.
The Clinical Trial Coordinator II provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, track study metrics, and maintain collaborative relationships with investigators and site personnel.
You will develop and implement business development strategies to identify and pursue new opportunities within the semiconductor industry. This role involves managing the full sales cycle, from lead generation to contract negotiation, while building strategic partnerships.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and coordinate with internal and external stakeholders to ensure trial activities meet quality standards.
You will partner with Global Regulatory Leads to develop and execute comprehensive regulatory strategies and integrated project plans across all stages of product development. Additionally, you will facilitate Global Regulatory Subteam meetings to ensure effective decision-making, risk mitigation, and cross-functional alignment.
The Senior CRA coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They also mentor junior team members and facilitate communication between investigative sites, the client, and the project team.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements and investigator grant budgets. They ensure compliance with company and client processes while managing risks and coordinating with internal teams to meet site activation timelines.
The Senior Technical Sales Specialist will drive revenue growth and customer success by applying technical expertise to identify opportunities and build strong client relationships. They will provide technical leadership, conduct product demonstrations, and act as a trusted advisor to help customers achieve their research and development goals.
The Lead DevOps Engineer will spearhead CI/CD strategy, infrastructure as code, and system performance optimization to support agile development. They will also manage container orchestration platforms and mentor junior engineers to ensure operational success.
The Data Reviewer ensures the integrity and quality of laboratory and chromatographic data by verifying compliance with analytical methods, SOPs, and GMP standards. They communicate findings to laboratory staff, prepare QC statements, and support process improvement initiatives.
The Country Approval Specialist manages and coordinates local regulatory submissions and provides regulatory strategy advice to internal clients. They also ensure site start-up activities align with submission timelines and maintain accurate trial status information in tracking databases.
The Account Director is responsible for acquiring and retaining high-value clients within the small and mid-sized pharmaceutical market. They will manage the entire sales process, including lead generation, proposal development, and negotiation to meet annual sales targets.
The Senior Manager will lead a team of clinical data management staff, overseeing performance, professional development, and project resourcing. They will ensure all clinical trial tasks are completed accurately, on time, and within budget while maintaining compliance with regulatory guidelines.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, maintain study documentation, and ensure compliance with regulatory standards and project protocols.
The Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They must provide exceptional customer service while ensuring all work adheres to safety protocols and quality standards.
The Principal Medical Writer is responsible for planning, coordinating, and delivering high-quality clinical and scientific documents such as IBs, INDs, and MAAs. They also provide senior-level review, mentorship to junior staff, and support project management activities to ensure operational excellence.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They oversee clinical monitoring, regulatory submissions, and team coordination to ensure compliance with study protocols and corporate policies.
The Senior Director will set global strategy and drive profitable growth across the OEM and Advanced Therapeutics commercial businesses. This role involves leading a global organization, managing key strategic accounts, and fostering cross-functional collaboration to execute consistent go-to-market approaches.
The Senior Director will define and execute the commercial strategy for the EMEA Clinical Sequencing business to achieve revenue and profitability targets. They will lead a diverse team, manage strategic customer relationships, and collaborate across divisions to drive market growth and operational excellence.
Lead patient-centric medical writing projects with a focus on Informed Consent Forms while managing timelines, budgets, and resources. Collaborate with cross-functional teams and clients to ensure high-quality deliverables and resolve project risks.
The Senior Manager will lead technology initiatives and digital transformation projects while ensuring regulatory compliance and audit readiness. They will partner with business leaders to develop strategic technology roadmaps and manage cross-functional teams across multiple locations.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Responsibilities include conducting site visits, verifying data accuracy, managing documentation, and resolving site-related issues to ensure subject safety and data reliability.
You will serve as a strategic talent advisor managing full-cycle recruitment for diverse roles across business units. This involves collaborating with hiring managers to develop sourcing strategies, build talent pipelines, and deliver an outstanding candidate experience.
You will drive growth and adoption of the molecular diagnostics portfolio by identifying market opportunities and developing evidence-based expansion strategies. Additionally, you will lead integrated marketing campaigns and create clinical education content to support global revenue targets.
You will drive revenue growth and customer success by providing technical sales expertise for scientific instruments and solutions. You will also manage key accounts and collaborate with cross-functional teams to implement effective sales strategies.
Serve as a primary scientific liaison between the company and laboratory customers to provide clinical education and support. Develop and maintain relationships with key opinion leaders and stakeholders to drive scientific partnerships and product adoption.
The Senior ICF Project Manager will lead patient-centric medical writing projects, specifically focusing on Informed Consent Forms (ICFs) through collaboration with internal and client teams. They are responsible for managing project timelines, budgets, resources, and ensuring the quality and timely delivery of all project documentation.
The Associate Financial Systems Analyst will support the administration, maintenance, and continuous improvement of Oracle Cloud ERP and related financial applications. They will collaborate with global stakeholders to troubleshoot issues, document requirements, and assist in the implementation of financial modules.
The Senior Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage project budgets, and ensure compliance with regulatory requirements and internal SOPs.
The Quality Manager is responsible for the operational execution of the Pharmacovigilance Quality Management System and driving continuous improvement within the Global Patient Safety area. Key duties include managing audit and inspection readiness, overseeing CAPA activities, and maintaining procedural documentation and training programs.
Provide expert installation, maintenance, and repair services for analytical and microscopy equipment across the Nordic region. Manage customer relationships, perform system certifications, and train users to ensure optimal performance of laboratory systems.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct remote or on-site visits to assess regulatory adherence and manage essential documentation throughout the clinical trial lifecycle.
The Senior CRA coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage documentation, and facilitate communication between investigative sites and project teams.
You will drive growth and adoption of the molecular diagnostics portfolio by creating market expansion strategies and evidence-based adoption frameworks. Additionally, you will lead integrated marketing campaigns and develop compelling content to translate complex clinical value into actionable demand generation programs.
The BioProduction Sales Specialist will drive growth and develop new business opportunities across the BioProduction portfolio within assigned accounts. They will manage primary customer relationships and coordinate with technical and applications teams to deliver comprehensive bioprocess solutions.
The Biostatistician II functions as a lead statistician responsible for statistical analysis, database creation, and the development of statistical analysis plans. They also lead project teams, manage budgets, and provide mentorship to junior staff members.
The Medical Director provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. They also manage safety variables, provide medical consultation to project teams, and assist in the review of clinical study reports and safety data.
The Account Executive is responsible for selling consumable and diagnostic lab supplies and instrumentation within a defined territory. They will manage strategic direction, maintain customer relations, and develop sales opportunities to meet or exceed sales objectives.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet project timelines.
Perform on-site installation, maintenance, and repairs of electron microscopes while providing technical support to customers. Coordinate work schedules and provide accurate service reports to ensure high levels of customer satisfaction.
Serve as a technical expert and consultant to support bioprocessing customers with process development, optimization, and technology integration. Lead pre- and post-sales technical activities while capturing customer insights to influence product roadmaps and innovation.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including document collection, system updates, and remote monitoring tasks. They assist in coordinating study activities, maintaining vendor trackers, and ensuring compliance with regulatory guidelines and SOPs.
The Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They will provide exceptional customer service and support while ensuring adherence to safety and quality standards in various laboratory environments.
The Clinical Research Associate ensures clinical studies are conducted in compliance with protocols, ICH-GCP, and local regulatory requirements. They are responsible for coordinating all aspects of the clinical monitoring process and ensuring the accuracy and integrity of study data.
The Account Manager will represent the company and manage the full sales process from pre- to after-sales support for molecular spectroscopy products. They are responsible for building long-term customer relationships, conducting product presentations, and managing sales opportunities within the assigned territory.
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They manage site processes, document observations, and facilitate communication between the sponsor and investigative sites throughout the clinical trial lifecycle.
The Sr Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and subject safety through risk-based monitoring. They will also manage site documentation, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial process.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage essential documentation in accordance with ICH-GCP guidelines.
The Senior Systems Developer serves as the technical lead for the Clarity PPM platform, providing L3 support and managing complex development, configuration, and integrations. They are responsible for resolving production issues, leading root-cause analysis, and ensuring technical standards are met across the support team.
The Application Administrator provides L2 operational support for the Clarity PPM platform, including incident resolution, service requests, and application monitoring. The role also involves maintaining system health, performing data-integrity checks, and supporting configuration and deployment activities.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform on-site and remote monitoring visits, manage documentation, and facilitate communication between investigative sites and project teams.
The CRA performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage documentation, and maintain collaborative relationships with investigational sites.
Performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. Conducts risk-based monitoring, manages essential documentation, and facilitates communication between investigative sites and the project team.
The Clinical Trial Coordinator II provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, perform file reviews, and maintain communication with investigators and internal departments to meet project timelines.
The Senior Medical Writer will serve as a primary author for complex clinical and regulatory documents, ensuring they meet industry standards and regulatory guidelines. They will also collaborate with cross-functional teams and provide mentorship to junior staff to ensure high-quality deliverables.
You will lead statistical tasks throughout the full clinical trial process, including study design, protocol writing, and final analysis. The role involves collaborating with clients and regulatory authorities to advance life-changing therapies.
The Country Approval Associate supports the preparation, review, and coordination of regulatory and ethical submissions in alignment with global strategies. They also assist with site start-up activities, budget negotiations, and the maintenance of trial status databases.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating investigator grant budgets and contractual terms with study sites. They coordinate with internal teams to ensure site startup activities align with contractual timelines and established risk management processes.
The associate will draft, review, and negotiate clinical trial site contracts and budgets while ensuring compliance with internal and client processes. They will also coordinate with internal functional departments to align site startup activities with contractual timelines.
The Account Executive will drive revenue growth and build lasting customer relationships by representing a portfolio of scientific products and services. They are responsible for prospecting new business, managing key accounts, and executing strategic sales plans within the assigned territory.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and company procedures. They act as the primary contact for study sites, driving performance and ensuring data quality throughout the study lifecycle.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring and issue resolution.
The Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements while ensuring compliance with budgetary and legal parameters. They will coordinate with internal teams to align site startup activities and manage risk throughout the contract lifecycle.
Manage the end-to-end supply chain for clinical trials to ensure timely distribution of materials and maintain optimal inventory levels. Collaborate with cross-functional teams to integrate supply chain activities with project logistics strategies and regulatory compliance.
The Key Account Executive is responsible for driving organic growth within strategic accounts by increasing share of wallet and expanding solution adoption. They serve as a trusted advisor to customers, aligning business objectives with enterprise solutions while coordinating cross-functional resources.
The Senior Clinical Data Team Lead acts as a primary liaison for clinical data management activities, overseeing project budgets, timelines, and study metrics. They are responsible for leading complex studies, delegating tasks, and mentoring junior staff to ensure operational excellence.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, perform file reviews, and maintain clinical trial databases while ensuring compliance with SOPs and regulatory guidelines.
The Fleet Administrator manages company car contracts, coordinates with leasing suppliers, and supports colleagues with vehicle inquiries via a case management system. They are also responsible for maintaining accurate fleet records, ensuring data compliance, and facilitating the full lifecycle of company car allocations.
Manage contract processes, documentation, and administration while collaborating with internal stakeholders to ensure smooth commercial operations. Coordinate with Account Managers and Legal teams to facilitate timely contract execution and maintain compliance with corporate policies.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal SOPs.
The Product Specialist will market controlled environment products within a designated territory to exceed sales forecasts and growth targets. They will collaborate with Laboratory Equipment Representatives to identify sales opportunities and maintain accurate CRM funnel reports.
The Principal Programmer Analyst provides strategic technical and validation leadership for complex Pharmacovigilance systems and initiatives. They ensure systems remain compliant, inspection-ready, and aligned with business objectives while driving process automation and continuous improvement.
The Associate Investigator Grant Analyst prepares, reviews, and finalizes global investigator grant budgets and payment schedules for clinical studies. They also liaise with clients and internal teams to negotiate budget parameters and ensure site startup activities align with project timelines.
Lead a sales team to drive revenue growth and market expansion for laboratory consumables and chemicals. Develop and implement strategic sales initiatives while fostering strong customer partnerships across a matrix organization.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Facilitates communication between investigative sites and project teams while managing trial documentation and site status reporting.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Facilitates communication between investigative sites, clients, and internal teams while managing trial documentation and site progress.
The Account Manager will support revenue growth and manage strategic relationships within the New Hampshire, Maine, and Boston markets. They will implement sales strategies, identify new business opportunities, and provide technical support for scientific product portfolios.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
The Account Manager III will develop and implement strategic sales plans while managing key account relationships to drive revenue. They will work with cross-functional teams to provide tailored scientific solutions and ensure customer satisfaction through consultative engagement.
The Senior Project Coordinator provides administrative and technical support to the Global Clinical Supplies team by managing project documentation, regulatory records, and data repositories. They also assist in project planning, coordinate team communications, and mentor junior staff to ensure compliance with GCP and project timelines.
The Principal Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities while ensuring site start-up activities meet critical path timelines.
The Regulatory Project Manager will lead strategic regulatory initiatives and ensure global compliance across medical devices, pharmaceuticals, and biologics. They will collaborate with cross-functional teams to manage product development, regulatory submissions, and lifecycle management.
Lead and develop a high-performing Site Payments team to ensure accurate, compliant, and timely investigator payments across clinical trials. Drive operational excellence by managing project delivery, mitigating risks, and implementing process improvements in collaboration with senior leadership.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
You will supervise technical support staff across IT disciplines including Desktop Services and Network Communications. You will drive service excellence through cross-functional partnerships while implementing technical solutions to meet business needs.
The Principal Regulatory Affairs Professional provides strategic regulatory guidance and intelligence to support product development from preclinical stages through registration. They also lead project teams, ensure compliance with global regulatory requirements, and act as a primary liaison for internal and external clients.
The Clinical Research Associate coordinates all aspects of the clinical monitoring and site management process to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
Develop and execute strategic sales plans to drive revenue growth and expand market share within assigned global biotech accounts. Build and maintain strong relationships with key client stakeholders while leading the RFP and RFI processes to secure new business opportunities.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also manage study documentation, facilitate cross-functional communication, and assist with process improvements and staff training.
Manages the complete life cycle of translation projects, including planning, scheduling, and risk management. Facilitates communication within the project team and maintains day-to-day relationships with clients.
You will serve as a technical expert providing comprehensive support, training, and troubleshooting for advanced scientific instrumentation. Additionally, you will collaborate with sales and R&D teams to optimize applications and drive business growth through customer engagement.
The position is responsible for securing revenue objectives for allergy and autoimmune products by prospecting and closing new business within a designated geographic territory. The role involves managing existing laboratory accounts and collaborating with internal divisions to drive clinical adoption and long-term growth.
Manage contract processes, documentation, and administration while collaborating with internal stakeholders to ensure smooth commercial operations. Coordinate with Account Managers and Legal teams to facilitate timely contract execution and ensure compliance with corporate policies.
Develop and grow the Bioproduction market in Denmark by managing the entire portfolio and implementing strategic sales plans. Collaborate with internal teams and field applications to drive sales objectives and provide technical support to key biopharmaceutical accounts.
Provide onsite service, including repairs, preventive maintenance, and installation of IDD analyzers at customer sites. Collaborate with internal partners and provide technical training to biomedical technicians and operators.
Perform on-site installation, preventive maintenance, and repair support for chromatography and mass spectrometry equipment at customer laboratories. Train customers on equipment operation and provide effective communication between the customer and the company.
The Senior Account Manager is responsible for driving sales and supporting the Chromatography and Mass Spectrometry Division portfolio within the assigned territory. This role involves developing strategic growth plans, managing customer relationships, and leading cross-functional teams to solve complex scientific challenges.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. This includes conducting site visits, verifying data accuracy, and managing documentation to guarantee subject rights and data reliability.
The Label Designer will develop and implement efficient labeling solutions while ensuring compliance with GMP and regulatory standards. The role involves collaborating with cross-functional teams to optimize labeling processes and maintain technical documentation.
The Senior Research Associate will lead scientific coordination and project management for de novo data collection projects, including drafting protocols and reports. They will also engage with clients, manage project budgets and timelines, and contribute to business development activities.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
The Account Manager will maintain and grow the Allergy and Autoimmune market by managing customer accounts and developing strong relationships across the assigned territory. Responsibilities include negotiating contracts, managing tenders, and collaborating with internal teams to ensure accurate forecasting and account planning.
The Field Service Engineer will install, maintain, troubleshoot, and repair complex analytical and scientific instruments across research, industrial, and healthcare settings. They are responsible for providing exceptional technical support, training customers on equipment operation, and documenting all service activities accurately.
The Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry products while maintaining long-term customer relationships. They will identify new client opportunities, negotiate contracts, and lead commercial activities within their assigned territory.
The Field Service Engineer will conduct on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and maintain detailed service reports while acting as a subject matter expert.
The Sr. Manager, Strategic Key Accounts is responsible for managing and expanding relationships with key customers in the global in vitro diagnostics market. This role involves leading commercial negotiations, developing strategic account plans, and coordinating cross-functional teams to drive revenue growth.
The Senior Portfolio Manager is responsible for the strategic and commercial management of a clinical diagnostics portfolio, including supplier relationship management and driving profitable growth. They will lead business reviews, negotiate commercial terms, and collaborate across internal teams to execute product launches and marketing initiatives.
The Field Service Engineer II is responsible for installing, maintaining, and repairing sophisticated analytical and scientific instrumentation at customer sites. They provide technical support, perform preventive maintenance, and ensure high levels of customer satisfaction through effective troubleshooting and communication.
The Sr. Manager, Strategic Key Accounts is responsible for managing and expanding relationships with key customers in the global in vitro diagnostics market. This role involves developing strategic account plans, leading commercial negotiations, and coordinating cross-functional teams to drive revenue and portfolio growth.
The Country Approval Associate manages and coordinates local regulatory submissions and site start-up activities in alignment with global strategies. They act as a key contact for regulatory and ethical submission-related activities while ensuring compliance with internal and client SOPs.
The Vendor Management Coordinator oversees clinical supply operations, including vendor coordination, purchase order management, and invoice reconciliation. They ensure all activities comply with company policies, GxP regulations, and project timelines while maintaining effective communication with internal stakeholders.
The Senior Clinical Trial Coordinator provides administrative and technical support to project teams while facilitating project activities and serving as a cross-functional liaison. They are responsible for maintaining study documentation, performing file reviews, and ensuring project tasks are completed on time and within budget.
The Clinical Trial Coordinator II provides administrative and technical support to project teams by facilitating project activities and acting as a cross-functional liaison. They are responsible for maintaining study documentation, performing file reviews, and ensuring tasks are completed on time and within budget.
The Site Compliance Lead manages the site compliance team to ensure adherence to legal, regulatory, and company policies. They drive operational quality initiatives, oversee quality management systems, and ensure accurate data reporting for clinical trials.
Develop and execute strategic territory plans to drive revenue growth and identify new business opportunities within the diagnostic market. Build and maintain strong relationships with healthcare professionals while providing consultative solutions that address clinical and operational needs.
The Safety Administrator coordinates the review of adverse events, protocol inquiries, and data for clinical trials while managing project documentation and committee logistics. They act as a liaison between internal teams, clients, and external vendors to ensure project timelines and safety standards are met.
The Clinical Trial Manager is responsible for achieving clinical deliverables within contractual time, quality, and cost expectations. They manage clinical operational aspects, lead study teams, and ensure compliance with ICH GCP and regulatory standards.
The Senior Safety Specialist performs day-to-day pharmacovigilance activities, including the collection, monitoring, and assessment of safety information. They also provide leadership, mentor junior staff, and ensure compliance with global regulatory requirements.
The Global Study Lead is responsible for the end-to-end operational management of global clinical studies, ensuring alignment between global strategy and regional execution. They lead cross-functional teams, manage CRO vendors, oversee study budgets, and ensure compliance with regulatory standards and quality requirements.
Develop and manage strategic customer relationships across a diverse portfolio of scientific products to drive revenue growth. Collaborate with technical specialists and product managers to deliver comprehensive solutions that meet complex customer research and manufacturing needs.
The Biostatistician will serve as a lead statistician for clinical research projects, overseeing statistical analyses, protocol design, and the development of analysis plans. They will also coordinate with data management and programming teams while ensuring compliance with departmental SOPs and project timelines.
You will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. This involves conducting on-site or remote visits, managing documentation, and resolving site-level issues to maintain audit readiness.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory requirements and internal SOPs.
Develop and manage relationships with academic and industry customers to achieve sales objectives for the Olink proteomics portfolio. Drive territory growth by identifying customer needs, providing technical solutions, and managing biomarker discovery projects.
Lead and execute global CMC regulatory strategies for biological products while ensuring compliance with US and Canadian regulatory requirements. Manage the preparation, review, and submission of regulatory dossiers and oversee post-approval lifecycle management activities.
The Site Contract Specialist manages the drafting, negotiation, and finalization of investigator contracts and budgets while ensuring compliance with company and client standards. They also coordinate with internal teams to align site startup activities with project timelines and provide mentorship to junior staff.
Provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. Manages safety variables, performs medical reviews of adverse events, and provides consultation to project teams and clients.
The representative will achieve territory revenue goals by proactively developing a sales pipeline and managing customer relationships. They will also collaborate with channel partners to promote the company's broad product portfolio and maximize business results.
The Senior Account Manager will drive revenue growth by promoting a comprehensive portfolio of analytical instruments and consumables to various scientific accounts. This field-based role involves developing strategic relationships with key decision-makers and coordinating cross-functional resources to provide exceptional customer experiences.
The Senior Patient Recruitment and Engagement Lead will provide strategic leadership for global patient recruitment and retention across clinical trials. This role involves managing recruitment campaigns, overseeing vendor performance, and collaborating with cross-functional teams to ensure enrollment success and quality data collection.
The Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry products while maintaining long-lasting customer relationships. They identify new client opportunities, negotiate contracts, and lead sales strategies to meet quarterly objectives within their assigned territory.
The Import/Export Coordinator manages the compliant movement of clinical supplies by coordinating with logistics providers, customs brokers, and internal teams. They are responsible for preparing shipping documentation, monitoring international shipments, and resolving any logistics or customs-related issues.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects in terms of quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
The Senior Site Contract Specialist manages the preparation, negotiation, and finalization of investigator contracts while ensuring compliance with legal and financial parameters. They also coordinate with internal teams to align site startup activities and provide mentorship to junior staff.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They manage site documentation, facilitate communication between stakeholders, and ensure trial materials are properly handled and reported.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and adherence to ICH-GCP guidelines. They manage site documentation, facilitate communication between stakeholders, and perform risk-based monitoring activities to ensure trial integrity.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage essential trial documentation.
You will develop and validate analytical applications while serving as a subject matter expert to support customer research and innovation. The role involves collaborating with R&D and commercial teams to translate customer needs into optimized scientific workflows.
You will drive market adoption of NGS library prep solutions by acting as a technical authority and consultative partner for research and clinical customers. Additionally, you will manage complex sales cycles and collaborate with internal teams to ensure seamless customer onboarding and revenue growth.
The Senior BioProduction Account Manager will own overall revenue, bookings, and account performance across all Thermo Fisher BioProduction business units within assigned customer sites. They will lead customer relationships, develop accurate forecasts, and coordinate integrated workflow solutions by collaborating with technical and product management teams.
The Senior Programmer Analyst leads bioinformatics programming activities for clinical research projects and manages data across multiple systems. They are also responsible for mentoring junior team members and contributing to departmental infrastructure and SOP development.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They will provide exceptional customer service while supporting customers across research, industrial, and healthcare settings.
The Medical Director provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. They also provide medical consultation to project teams, monitor safety variables, and review serious adverse events.
The Clinical Program Quality Excellence Lead manages cross-functional teams to ensure GCP inspection readiness and high-quality deliverables throughout the clinical study lifecycle. They provide guidance on operational processes, oversee TMF performance, and facilitate audit and inspection preparation.
Lead global labeling strategy and author key regulatory documents such as the Target Product Label and Company Core Data Sheet. Act as a subject matter expert and liaison between internal teams, external clients, and health authorities to ensure regulatory compliance and high-quality submissions.
The Customer Success Manager is responsible for selling service products, such as maintenance contracts and warranty extensions, to existing and new customers. They will manage contract renewals, build long-term client relationships, and utilize CRM systems to track sales activities and achieve financial targets.
The role involves coordinating clinical monitoring and site management processes to ensure trial compliance with protocols, ICH GCP guidelines, and regulatory standards. Responsibilities include conducting risk-based monitoring, verifying data accuracy, and maintaining collaborative relationships with investigator sites.
The Global Study Lead is responsible for the end-to-end management of global clinical studies, ensuring alignment between global strategy and regional execution. They lead cross-functional teams, manage CRO vendors, and oversee study budgets, timelines, and regulatory compliance.
Develop and implement strategic sales plans to drive the adoption of diagnostic testing and manage key account relationships. Collaborate with cross-functional teams to provide tailored solutions while ensuring customer satisfaction and achieving sales targets.
The Senior Manager will lead a portfolio of applied AI initiatives, overseeing technical design, development, and production deployment across generative and agentic AI. They will also coach multidisciplinary teams and drive the creation of reusable enterprise AI capabilities to ensure scalable and reliable business solutions.
The Project Manager serves as the primary lead for non-interventional clinical trials, ensuring the project is delivered on time, within budget, and to high quality standards. They are responsible for managing cross-functional teams, maintaining sponsor relationships, and ensuring compliance with regulatory requirements and internal SOPs.
Conduct and manage internal and external clinical audits, identify quality and compliance issues, determine root causes, and develop corrective strategies. Report audit findings, lead quality improvement initiatives, develop compliance tracking tools, and mentor staff while supporting clinical development programs.
The Expanded Access Manager will lead the operational support for post-trial managed access programs, including budget coordination and vendor management. They will collaborate with cross-functional teams to ensure regulatory compliance and continuity of access for patients.
The Global Study Manager is accountable for the end-to-end operational delivery of clinical studies, ensuring they meet time, quality, and budget targets. They lead matrix teams, manage vendors, and oversee risk mitigation strategies throughout the study lifecycle.
The Field Application Scientist provides technical training, application support, and pre-sales consultation for HID products across Western North America. They collaborate with internal teams and customers to ensure successful implementation and optimization of forensic workflows.
You will identify and pursue new business opportunities while developing strategic relationships with key accounts to drive growth. Additionally, you will collaborate across divisions to deliver comprehensive solutions and manage the sales pipeline through the CRM system.
You will lead a sales team to drive customer success and business growth while executing strategic sales plans across research and clinical markets. Additionally, you will maintain strong customer relationships, analyze market trends, and ensure the team meets or exceeds sales and profitability targets.
You will be responsible for the configuration, implementation, and deployment of Thermo Scientific SampleManager LIMS solutions across various laboratory environments. This involves translating functional requirements into technical workflows, managing system integrations, and supporting data migration and validation activities.
You will serve as a technical expert in downstream bioproduction, providing comprehensive support, training, and troubleshooting for customers. Additionally, you will collaborate with internal R&D teams to provide feedback and contribute to product development and strategic projects.
The Director of Product Specialists will lead product strategy and oversee the performance of product specialist teams. This role involves driving business results through effective team management and cross-functional collaboration.
The Customer Service Representative will handle customer inquiries and provide support in a professional manner. They are responsible for maintaining accurate records and ensuring high levels of customer satisfaction.
The manager will oversee product support operations and ensure high-quality service delivery for the company's product lines. They are responsible for leading the support team and coordinating with internal departments to resolve complex customer issues.
The manager will oversee product support operations to ensure high-quality service delivery. They are responsible for managing team performance and maintaining standard office workflows.
The role involves performing standard customer service representative duties. The position operates on a standard Monday through Friday schedule.
Drive sales growth and manage key accounts across academic, government, and industrial sectors within the assigned territory. Execute strategic sales initiatives, maintain a healthy sales pipeline, and build strong relationships with key stakeholders to achieve revenue targets.
The Medical Director provides medical oversight for clinical trials, ensuring adherence to regulatory requirements and company SOPs. They also manage safety profiles, perform medical reviews of adverse events, and provide consultation to investigators and project teams.
Provide technical support including installation, preventative maintenance, and repair of laboratory equipment while managing customer relationships. Lead commissioning and qualification protocols and ensure timely service delivery and performance metrics are met.
Oversee end-to-end clinical study delivery, including study plans, vendors and CROs, country progress, budgets, supplies, risks, and cross-functional team communications. Maintain inspection readiness through oversight of study data and eTMF completeness, while resolving or escalating delivery issues and mentoring colleagues.
The Country Approval Specialist manages and coordinates local regulatory submissions and provides strategic regulatory advice to internal clients. They also ensure site start-up activities align with submission timelines and maintain accurate trial status documentation.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet project timelines.
Manage all clinical operational and quality aspects of allocated studies of moderate to high complexity in compliance with ICH GCP. Ensure clinical deliverables meet customer time, quality, and cost expectations while maintaining project profitability.
The Pharmacovigilance Coordinator manages safety documentation, tracks adverse events, and coordinates project meetings for global clinical trials. They also interface with internal and external stakeholders to ensure audit readiness and compliance with regulatory standards.
The Account Manager II will support revenue growth by developing and maintaining strategic customer relationships while promoting a portfolio of scientific products. They will implement sales strategies, identify new business opportunities, and provide excellent support to help customers achieve their goals.
The Account Manager is responsible for selling and supporting chromatography and mass spectrometry products while maintaining long-term customer relationships. They will identify new client opportunities, negotiate contracts, and lead sales strategies to meet quarterly objectives within their assigned territory.
The Site Contract Specialist will draft, review, and negotiate clinical trial agreements and investigator grant budgets with study sites. They will also coordinate with internal functional teams to ensure site activation timelines are met while managing legal and financial risks.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities to ensure timely site activation and compliance.
The Business Development Associate will act as the initial touchpoint for new customers to identify and qualify business opportunities within the pharmaceutical industry. They will support outbound campaigns, manage CDA/NDA execution, and coordinate client meetings to build a strong pipeline of prospects.
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, oversee project financials, and ensure compliance with ICH GCP and regulatory standards throughout the study lifecycle.
The Site Account Representative will manage on-site asset management and laboratory support services for key customer accounts. They will serve as the primary point of contact to ensure seamless service delivery and high customer satisfaction.
The Technical Sales Specialist is responsible for driving revenue growth for mass spectrometry and chromatography products by identifying new opportunities and supporting account managers. They act as a technical advisor to customers, managing the sales process from initial prospecting through to deal closure.
The Procurement Assistant is responsible for managing purchase requisitions, purchase orders, and vendor invoices within the Global Clinical Supplies Team. They also ensure financial tracking accuracy and resolve procurement-related discrepancies in collaboration with cross-functional teams.
The Senior Clinical Team Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory standards.
The Import/Export Coordinator is responsible for planning and executing complex import and export activities for clinical studies. They ensure all logistics are compliant with PPD, client requirements, and global regulations while maintaining accurate metrics and documentation.
The Clinical Research Associate will perform and coordinate all aspects of the clinical monitoring process while working within multi-national project teams. They are responsible for ensuring high levels of customer service and maintaining quality and accuracy across multiple clinical research projects.
The Clinical Sales Specialist will drive revenue growth and develop new business opportunities within hospitals and laboratories across the assigned territory. They will serve as a trusted advisor by applying a consultative approach to understand customer needs and provide tailored diagnostic solutions.
The Associate Manager Clinical Operations oversees daily line management, coaching, and professional development for clinical operations staff. They collaborate with senior management on strategic planning, resource allocation, and ensuring adherence to company SOPs and quality standards.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage clinical trial documentation, perform file reviews, and coordinate with internal and external stakeholders to meet project timelines.
The Market Development Specialist identifies and develops commercial growth opportunities for Precision Diagnostics solutions by engaging healthcare providers and partners. They manage a defined book of business, monitor adoption data, and collaborate across internal teams to drive sustained utilization and market expansion.
The Demand and Supply Manager will design and implement inventory management plans to forecast supply for global clinical trials using sound supply chain techniques. They will also partner with cross-functional teams to optimize supply strategies and ensure continuity of subject supply while managing financial forecasts.
You will perform and coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Additionally, you will manage site relationships, conduct risk-based monitoring, and mentor junior team members to ensure data reliability and audit readiness.
Performs and coordinates all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data accuracy, manage documentation, and maintain collaborative relationships with investigational sites.
Provides administrative and technical support to the project team, including site activation activities and audit readiness. Manages clinical trial documentation, ensures system databases are current, and coordinates with internal departments to meet project deadlines.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include verifying document collection, managing site supplies, and assisting with study-specific systems and vendor coordination.
The Clinical Data Team Lead acts as the primary data manager for clinical studies, overseeing data management activities and ensuring operational excellence. They serve as a liaison between the project team and clients while mentoring junior staff and managing project documentation.
The Operations Strategy Consultant manages the proposal development process to increase RFP hit rates and business growth. They are responsible for defining operational strategies, overseeing budgets, and collaborating with cross-functional teams to ensure successful clinical trial project delivery.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
The Biostatistician II acts as a lead statistician, independently managing analysis database creation, statistical programming, and the development of analysis plans. They also provide mentorship to junior team members and coordinate directly with sponsors and project teams to ensure adherence to statistical methodology and project timelines.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence using a risk-based approach. They will manage site processes, facilitate communication between stakeholders, and ensure trial documentation is complete and audit-ready.
You will drive revenue growth by promoting a portfolio of analytical instruments and consumables to key decision-makers. This role involves managing complex sales cycles and building strategic relationships across government, academic, clinical, and industrial sectors.
The Strategic Account Manager is responsible for driving reagent revenue growth and customer retention across a portfolio of laboratory accounts. They will develop strategic account plans and serve as the primary point of contact for stakeholders in hospitals, reference labs, and integrated health systems.
Perform on-site installation, preventive maintenance, and repairs of electron microscopy systems while providing technical support to customers. Coordinate work schedules and ensure high levels of customer satisfaction through effective communication and reporting.
The QA Auditor II will conduct and lead various client, internal, and GCP audits while ensuring regulatory compliance and quality standards. They will also provide GCP consultation to project teams and prepare audit findings for internal and client meetings.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
Provide post-sales technical support through training, troubleshooting, and workflow optimization for pharmaceutical analytics solutions. Collaborate with customers to implement solutions while acting as a customer advocate to influence product improvements and support sales activities.
The Senior Clinical Trial Manager is responsible for managing all clinical and start-up activities, ensuring projects meet quality, time, and cost expectations. They act as the primary point of contact for sponsors and coordinate cross-functional teams to drive operational excellence in clinical trials.
The Compliance Manager will lead and manage GxP audits and regulatory inspections for clinical trials across the APAC region. They will provide consultation on inspection readiness, facilitate audit hosting, and support project teams in developing CAPAs to address non-conformances.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage essential trial documentation.
The Clinical Research Associate coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-related issues.
Lead and develop a team of Clinical Sales Specialists to drive allergy testing growth and optimize lab utilization across the assigned district. Develop and execute strategic sales plans while cultivating advocacy and maintaining strong relationships with key healthcare decision-makers.
The Technical Sales Specialist will develop and execute business strategies for the Cell Culture and Cell Therapy portfolio across the Nordic region. They will drive new business opportunities, manage customer relationships, and collaborate with internal teams to provide technical solutions for bioprocessing workflows.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, maintain study documentation, and ensure compliance with ICH GCP and regulatory requirements.
The Senior Clinical Research Associate ensures clinical studies are conducted in compliance with protocols, ICH GCP, and regulatory requirements. They perform and coordinate all aspects of the clinical monitoring process to ensure data accuracy and subject safety.
Manage clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulatory standards. Perform site monitoring activities, maintain inspection readiness, and collaborate with project teams to deliver high-quality clinical trials.
The Business Development Executive is responsible for driving profitable growth by securing new molecules and expanding services within assigned biotech accounts. They will execute territory sales plans, manage the sales cycle from outreach to contract execution, and collaborate cross-functionally to deliver integrated solutions.
You will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. This includes conducting on-site or remote visits, performing root cause analysis, and managing corrective actions to maintain audit readiness.
The Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site or remote visits, manage documentation, and facilitate communication between investigative sites and the project team.
The Senior Medical Director will provide medical monitoring and safety evaluation for clinical trials within the pharmacovigilance department. They will also lead medical aspects of contracted tasks and support business development activities by presenting safety processes to clients.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data reliability through rigorous review and problem-solving.
The Senior Account Manager will drive profitable growth by developing strategic customer relationships and managing the full sales cycle for materials and surface analysis solutions. They will collaborate with technical and service teams to identify customer needs, respond to tenders, and provide effective product and workflow recommendations.
The Project Budget Coordinator will manage clinical trial budgets, track indirect costs, and provide financial reporting for project teams. They will also coordinate cross-functional activities and handle purchase requisitions within the clinical supplies lifecycle.
The Field Service Engineer will install, maintain, troubleshoot, and repair complex analytical instruments such as SEM and SDB systems. They are responsible for providing exceptional customer service and training while documenting all service activities.
The Senior Sales Manager will lead and develop commercial teams to drive strategic growth and achieve revenue targets within the Southeast region. They are responsible for implementing sales strategies, managing pipelines, and fostering strong customer relationships across the life sciences portfolio.
You will represent a portfolio of scientific instruments and solutions to drive revenue growth and customer success. As a technical advisor, you will collaborate with cross-functional teams to implement sales strategies and provide expertise throughout the sales cycle.
Provide onsite service including repairs, preventive maintenance, and installation of IDD analyzers at customer sites. Collaborate with internal partners and provide technical training to Biomedical Engineering Technicians and operators.
Provides medical oversight for clinical trials, ensuring adherence to regulatory requirements, SOPs, and good clinical practices. Manages safety variables, performs medical reviews of adverse events, and provides medical consultation to project teams and investigators.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform on-site and remote monitoring activities, manage documentation, and resolve site-related issues to ensure data reliability and subject safety.
The role involves coordinating all aspects of clinical monitoring and site management to ensure trials are conducted according to protocols and ICH-GCP guidelines. You will perform risk-based monitoring, ensure data accuracy, and maintain collaborative relationships with investigational sites.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data accuracy through rigorous review processes.
The Global Study Manager will lead the operational strategy and end-to-end delivery of complex global clinical studies, ensuring adherence to timelines, budget, and quality standards. They will provide strategic leadership to cross-functional teams and act as the primary escalation point for operational issues.
You will coordinate all aspects of clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. This includes conducting on-site or remote visits, managing documentation, and performing data verification to ensure subject safety and data reliability.
The Clinical Specialist will support business growth through technical sales expertise, customer relationship management, and strategic sales initiatives. They are responsible for conducting product demonstrations, providing application support, and managing contract implementations to advance laboratory research.
Provides nutrition expertise and operational support for clinical trial nutrition programs, including menu development and lifestyle intervention services. Collaborates with internal teams and stakeholders to ensure regulatory compliance and high-quality execution of study requirements.
The specialist will manage account profiling and develop relationships with key healthcare stakeholders to drive procalcitonin testing strategies. They are responsible for delivering clinical education programs and meeting annual operating growth targets within their designated region.
Drive clinical demand and adoption of Procalcitonin and other innovative biomarkers through engagement with healthcare professionals. Develop hospitals and healthcare institutions by building relationships and supporting the implementation of biomarker-guided clinical pathways.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include maintaining study documentation, coordinating vendor data, and assisting with site preparedness and patient-facing materials.
The Account Manager will drive commercial growth by developing strategic territory plans and managing relationships with clinical laboratories and key decision-makers. They are responsible for the full sales cycle, from identifying new business opportunities to closing deals and ensuring long-term customer satisfaction.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between internal teams and clinical sites.
The Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety data, perform signal detection, and provide medical consultation to project teams and clients.
Perform on-site installation, maintenance, troubleshooting, and repair of complex IC-LC-MS analytical instruments. Actively promote service contracts and maintain strong customer relationships while ensuring compliance with safety and quality standards.
The Senior Manager will oversee clinical data management staff, including performance management, coaching, and resource allocation. They will also ensure operational quality and compliance with procedures while supporting study portfolios to meet client expectations.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring visits and system updates.
The Field Application Scientist will serve as a technical expert to support customers in adopting single-use upstream bioprocessing technologies and optimizing workflows. They will lead pre- and post-sales technical activities, provide troubleshooting, and deliver training to ensure customer success and regulatory compliance.
The Business Development Executive is responsible for driving growth within health systems and laboratories by advancing the adoption of diagnostic testing solutions. This role involves managing the transition from onboarding to revenue realization while orchestrating internal resources to meet sales targets.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They are responsible for conducting site visits, managing documentation, and facilitating communication between investigative sites and the project team.
The Clinical Data Team Lead acts as the primary data manager for clinical studies, overseeing data management activities and ensuring operational excellence. They serve as a liaison between departments and clients while mentoring junior staff and managing project documentation and metrics.
The Senior Site Contract Specialist manages the drafting, negotiation, and finalization of investigator agreements while ensuring compliance with budgetary and contractual parameters. They also coordinate with internal teams to align site startup activities and provide mentorship to junior staff.
The Global Cold Chain & HVAC Leader provides technical leadership and functional expertise to establish global engineering standards for temperature-controlled storage and HVAC systems. This role drives network capability, manages capital planning, and ensures compliance and business continuity across the CTD network.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including site preparedness, remote monitoring, and document collection. They also assist with system updates, vendor coordination, and reconciliation tasks to ensure compliance with SOPs and regulatory guidelines.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They will also manage site processes, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial lifecycle.
Lead and oversee complex clinical trial start-up activities across multiple EU countries while ensuring adherence to regulatory requirements and project timelines. Manage cross-functional stakeholders, site activation processes, and financial/contractual aspects to ensure successful study delivery.
The Associate Director will lead EU regulatory strategy and provide expert guidance throughout the product lifecycle, from preclinical stages to post-approval. They will act as a key liaison between internal teams and regulatory authorities to ensure high-quality, timely submissions and compliance.
The Director of Project Management will oversee complex, cross-functional strategic initiatives to drive business growth and operational efficiency. This role involves establishing project governance frameworks and leading teams to deliver results aligned with corporate objectives.
The specialist will proactively build and cultivate relationships with physicians, healthcare professionals, and community leaders to drive clinical trial recruitment. They will manage regional outreach activities, attend community events, and collaborate with internal teams to meet enrollment objectives.
Drive sales growth in the clinical trials division by developing and implementing strategies to generate business from new and existing biotech accounts. Manage the full sales cycle, including lead generation, contract negotiation, and maintaining strategic relationships with key opinion leaders and C-suite executives.
The Senior Account Manager will increase revenue by managing strategic customer relationships and serving as a trusted advisor for scientific products. They will collaborate with technical and support teams to deliver comprehensive solutions that advance critical research and manufacturing initiatives.
Manages complex translation project lifecycles, including planning, scheduling, and risk management. Facilitates communication between project teams and clients while ensuring financial and administrative processes are completed.
The Field Service Engineer II is responsible for the installation, maintenance, troubleshooting, and repair of sophisticated analytical instrumentation across a multi-state territory. They will provide high-quality technical support to customers in various laboratory settings to ensure optimal instrument performance and minimize downtime.
The developer will contribute to data acquisition, modeling, and mapping projects while supporting global business functions with reporting and analytics deliverables. They are also responsible for maintaining technical documentation, automating repetitive tasks, and providing support for operational incidents.
The role involves developing and integrating AI and data solutions using Databricks, SAP, and cloud AI services. You will also design ETL pipelines, automate data workflows, and provide operational support for data systems.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal SOPs.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial agreements and investigator grant budgets with study sites. They ensure compliance with internal processes and client expectations while coordinating with functional teams to meet site activation timelines.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal SOPs.
The Field Service Supervisor will lead and support a team of field service engineers to ensure exceptional service delivery and operational excellence. This role involves coordinating service activities, managing team performance, and maintaining strong relationships with customers and internal stakeholders.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The Drug Safety Specialist performs daily pharmacovigilance activities including data entry, coding, and the assessment of adverse events. They also coordinate regulatory reporting, maintain safety databases, and collaborate with project teams and investigators.
The Safety Reporting Coordinator provides administrative support for pharmacovigilance, including the submission, tracking, and archiving of safety reports. They also assist with audit readiness, reconcile clinical trial data, and train staff on safety reporting processes.
The Assistant Clinical Research Associate provides logistical and administrative support for site preparedness, study start-up, and remote monitoring activities. They collaborate with clinical teams to ensure data accuracy, regulatory compliance, and efficient execution of clinical trial protocols.
The Qualified Person for Pharmacovigilance acts as the EU/UK QPPV for selected clients, ensuring compliance with EU Directive 2001/83/EC and associated regulatory guidance. They also contribute to scientific safety services, manage budgets, and promote QPPV services to potential clients.
The Technical Sales Specialist is responsible for driving revenue growth for HPLC products by identifying new client opportunities and supporting account managers. They act as a technical advisor throughout the sales cycle, from prospecting to closing, while providing product expertise and training to internal teams.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
Conduct and lead various GCP, client, and internal audits to ensure regulatory compliance and quality standards. Serve as a knowledgeable resource for operational departments and provide GCP consultation to project teams.
The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and facilitate communication between investigative sites and the project team.
You will coordinate all aspects of clinical monitoring and site management to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting remote or on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The Field Service Engineer II is responsible for the installation, maintenance, troubleshooting, and repair of sophisticated analytical instruments like SEM, TEM, and FIB systems. They must provide exceptional customer service, conduct on-site training, and travel to customer sites to resolve technical issues.
Perform on-site installation, maintenance, troubleshooting, and repair of complex IC-LC-MS analytical instruments. Ensure high customer satisfaction while managing spare parts inventory and promoting service contracts.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
The Field Application Scientist provides onsite technical support for purification products, assisting customers with process development, optimization, and troubleshooting. They also collaborate with sales and technical teams to drive product adoption and gather market feedback.
The Recruitment Specialist will manage full-cycle recruitment for diverse roles while serving as a strategic talent advisor to hiring managers. They will develop effective sourcing strategies, build talent pipelines, and ensure a positive candidate experience across business units.
The specialist will drive revenue growth by managing technical sales for ion chromatography products and acting as a trusted advisor to key accounts. They will collaborate with cross-functional teams to implement sales strategies, support new product introductions, and provide technical expertise throughout the sales cycle.
Provide medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. Conduct medical review and analysis of safety data, including serious adverse events and periodic safety reports.
The Assistant CRA provides remote support for clinical trial site preparedness, monitoring activities, and site management tasks. They ensure regulatory compliance, manage study documentation, and coordinate logistics for site staff and vendor activities.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage documentation to maintain audit readiness.
The Technical Sales Specialist is responsible for driving sales and providing technical support for flow cytometry analyzers and cell sorters within academic, government, and industrial accounts. This role involves prospecting for new business, conducting instrument demonstrations, and representing the company at scientific trade shows and events.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
Provides strategic leadership for clinical trial nutrition programs, including program design, implementation, and vendor management. Leads cross-functional teams to ensure regulatory compliance and operational excellence across regional and multi-site studies.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
Manage full-cycle recruitment for commercial and operations roles across Israel, the Middle East, and Africa. Collaborate with stakeholders to drive data-informed hiring strategies and process improvements.
The Lead Account Manager will drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. They will build strategic relationships with key decision-makers to position the company as a preferred provider for life-changing therapies.
The Associate Site Activation Specialist manages the critical path for site activation to ensure rapid project implementation and regulatory compliance. They act as a subject matter expert, providing technical guidance and coordinating with internal departments to align site startup activities.
Develop and execute territory plans to drive profitable growth for the PPA portfolio in the mining, metals, and cement industries. Build and maintain strategic customer relationships while managing complex consultative sales cycles from identification to closure.
Provide medical oversight for clinical trials, ensuring adherence to regulatory requirements and company SOPs. Conduct medical review and analysis of safety data, including serious adverse events and periodic safety reports.
The Customer Success Manager is responsible for selling service products, including warranty extensions and maintenance contracts, while managing customer relationships. They will also handle contract renewals, prepare sales reports, and collaborate with internal teams to achieve financial targets.
The Senior Key Account Manager is responsible for driving sales strategies and managing account activities for Life Science Electron Microscopy products within the assigned territory. They will lead sales efforts, maintain accurate booking forecasts, and build professional networks within the pharma and biotech sectors to achieve business goals.
Drive profitable sales growth by managing biotech accounts and executing territory plans across various drug modalities. Build and maintain strong customer relationships while collaborating cross-functionally to deliver integrated solutions.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs for clinical projects to ensure efficient labor utilization. They also coordinate project team compositions, manage resourcing reports, and liaise with internal departments to support business goals and project authorizations.
The Senior Research Associate leads scientific coordination, project management, and the design of de novo data collection projects. They are responsible for drafting scientific deliverables, engaging with project stakeholders, and contributing to business development activities.
The Procurement Assistant will support procurement operations and administrative tasks. The role involves managing standard office-based procurement workflows.
You will lead the Professional Services business for DSAS, overseeing revenue delivery, operational execution, and project governance. Additionally, you will collaborate with cross-functional teams to deliver comprehensive LIMS solutions while ensuring high customer satisfaction and cost control.
Provide expert installation, maintenance, and repair services for sophisticated laboratory automation equipment and dynamic scheduler software. Build strong customer relationships while ensuring optimal system performance through preventive maintenance and user training.
Define and govern the rare disease portfolio strategy while leading high-value executive client engagements and bid defenses. Partner with cross-functional leadership to convert scientific strategy into measurable revenue, quality, and delivery outcomes.
The Senior Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of global Oncology/Hematology trials regarding quality, time, and cost. They lead cross-functional teams, manage project risks, and ensure compliance with regulatory requirements and internal SOPs.
The Innovation Technologist designs and delivers end-to-end digital solutions by integrating full-stack development, data engineering, and AI/ML capabilities. They collaborate with cross-functional stakeholders to ensure solutions meet clinical, regulatory, and business requirements.
The Global Study Lead provides strategic and operational leadership for the end-to-end delivery of global clinical studies, with a specific focus on Managed Access Programs. They are responsible for managing study timelines, budgets, quality, and cross-functional teams while serving as the primary escalation point for clinical operations.
The Clinical Research Associate monitors investigator sites to ensure protocol and regulatory compliance using a risk-based approach. They are responsible for managing site documentation, verifying data accuracy, and facilitating communication between investigative sites and the project team.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Manages site relationships and conducts remote or on-site visits to assess regulatory adherence and audit readiness.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage documentation to ensure data reliability and subject safety.
The Strategic Account Manager is responsible for driving reagent revenue growth and customer retention across a defined portfolio of laboratory accounts. They will develop strategic account plans and serve as the primary point of contact between customer stakeholders and internal commercial partners.
The Sr. Safety Specialist is responsible for driving sales of safety products and services within a defined territory to industrial and medical customers. They will develop sales strategies, conduct hazard assessments, and maintain strong relationships with purchasing and end-user stakeholders.
The Lead Biostatistician will serve as the statistical lead for pharmacovigilance and safety-focused projects, designing studies and developing statistical analysis plans. They will also oversee and mentor junior staff while collaborating with cross-functional teams to ensure high-quality real-world evidence generation.
The Regulatory Affairs Specialist will manage CMC compliance activities, including change controls, deviations, and regulatory submissions. They will collaborate with cross-functional teams to ensure product registrations and documentation meet global regulatory requirements.
The Global Regulatory Lead will develop and execute global regulatory strategies while serving as a key business partner for product life cycle management. This role involves coordinating regulatory filings, overseeing vendors, and ensuring timely compliance with global health authority requirements.
The NGS Sales Specialist will drive revenue growth by strategically selling advanced scientific instruments and managing key customer relationships across research, pharmaceutical, and industrial sectors. They will collaborate with cross-functional teams to identify opportunities and deliver customized solutions that meet customer needs.
The Senior Clinical Sales Specialist will drive revenue growth and develop new business opportunities within hospitals and laboratories. They will serve as a trusted advisor by applying a consultative approach to understand customer needs and provide tailored clinical diagnostic solutions.
The Field Service Engineer will install, maintain, and repair a diverse range of high-value analytical instruments to ensure peak performance. They will act as a company representative, delivering exceptional technical service and building strong relationships with customers.
The Sales Representative will develop and maintain strategic customer relationships while promoting a portfolio of scientific products and services. They are responsible for implementing sales strategies, identifying new business opportunities, and providing support to help customers achieve their goals.
The Benefit-Risk Excellence Lead will drive innovation and digital transformation within the BRAMS function by leading strategic projects and process improvements. They are responsible for governance, portfolio prioritization, and ensuring effective communication between business stakeholders and technology teams.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They provide exceptional customer service and support to clients across research, industrial, and healthcare settings.
The Medical Writer is responsible for planning, coordinating, and producing high-quality clinical and scientific documents such as study reports and protocols. They also collaborate with internal and external clients to ensure operational excellence and compliance with quality standards.
The Project Support Specialist is responsible for managing operational metrics, ensuring audit readiness, and supporting departmental process improvements. They provide end-to-end oversight of study-level activities and maintain high training compliance across functional departments.
Field Service Engineers manage customer relationships and provide technical support, including installation, repairs, and preventative maintenance of chromatography and mass spectrometry equipment. They are responsible for meeting service level agreements and internal key performance indicators while ensuring high levels of customer satisfaction.
The Field Service Engineer will conduct on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and act as a subject matter expert for system troubleshooting and documentation.
The Senior Recruiter will manage full-cycle recruitment for diverse roles while acting as a strategic talent advisor to business partners. They are responsible for developing sourcing strategies, building talent pipelines, and providing data-driven insights to hiring managers.
The Supervisor will lead a team of Field Service Engineers, managing their performance, development, and daily scheduling. They will also facilitate team communication, handle customer escalations, and perform field service activities for approximately 50% of their working hours.
You will lead and support a team of field service engineers to ensure high-quality service delivery and operational excellence. The role involves coordinating service activities, managing team performance, and maintaining strong relationships with customers and internal stakeholders.
The Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions and site start-up activities. They also lead complex site contract and budget negotiations while ensuring compliance with global and local regulatory standards.
Provide technical support, training, and scientific expertise for IC and HPLC analytical solutions to customers. Collaborate with cross-functional teams to optimize customer workflows, conduct product demonstrations, and drive business growth.
The Technical Sales Specialist is responsible for driving revenue growth for chromatography and mass spectrometry products by identifying new client opportunities and supporting account managers. They act as a trusted advisor to customers, managing the entire sales cycle from prospecting to closing while providing technical expertise.
You will coordinate clinical monitoring and site management processes to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting on-site or remote visits, managing documentation, and performing root cause analysis to mitigate risks and ensure data reliability.
The specialist will coordinate and manage the quality of clinical translations while maintaining terminology and style guides. They will also perform quality checks on clinical documents and monitor the performance of external language suppliers using CAT technology.
Develop and implement strategic sales plans for Olink Proteomics workflows while managing key account relationships. Serve as a trusted advisor to customers through consultative selling to help them achieve their scientific goals.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage essential documentation to guarantee data reliability and subject well-being.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They will also manage site documentation, facilitate communication between stakeholders, and participate in investigator meetings and trial close-out activities.
The PV Coordinator manages safety documentation, coordinates protocol inquiries, and facilitates meetings for clinical trials and safety boards. They also ensure audit readiness, perform data entry, and maintain effective communication with internal and external project stakeholders.
The Account Manager is responsible for selling service contracts for chromatography and molecular scientific equipment within the French territory. They will focus on exceeding sales quotas, developing account-specific strategies, and collaborating with cross-functional teams to drive growth.
The Clinical Data Manager Project Manager oversees the functional, administrative, and financial aspects of clinical studies or programs. They are responsible for leading project teams, managing budgets, mitigating risks, and ensuring deliverables meet client expectations.
You will develop and implement strategic sales plans to increase revenue while managing key account relationships across the Upper Midwest. By serving as a trusted advisor, you will provide tailored scientific solutions to help customers achieve their goals.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, manage documentation, and facilitate communication between investigative sites and the project team.
Provide logistical and administrative support for site preparedness and remote monitoring in accordance with SOPs and regulatory guidelines. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
Monitor investigator sites using a risk-based approach to ensure data accuracy and compliance with protocols and regulatory requirements. Manage site initiation, close-out, and maintain regular communication with investigative sites to resolve deficiencies.
The role involves coordinating clinical monitoring and site management processes to ensure trial compliance with protocols and ICH-GCP guidelines. Key duties include conducting remote or on-site visits, performing data verification, and managing relationships with investigational sites.
The role focuses on completing investigator payment reconciliations in adherence to contractual guidelines and country regulations. Responsibilities include compiling patient activity data, managing bi-annual and final reconciliations, and resolving payment-related issues.
Accountable for the end-to-end operational delivery of global clinical studies, ensuring they are completed on time, within budget, and according to quality standards. This includes managing study plans, overseeing vendors, and leading matrix teams to achieve study deliverables.
Manages and coordinates medical projects to ensure compliance and optimal performance throughout the project lifecycle. Performs safety data reviews, manages project financials, and serves as the primary point of contact for clinical project teams.
Provide administrative and technical support for clinical trials, focusing on regulatory inspection readiness and site activation activities. Collaborate with study managers and CROs to manage study documentation, CTMS/TMF activities, and study close-out processes.
Provide administrative and technical support for clinical trials, including file reviews and system maintenance of eTMF and Activate. Coordinate site activation, regulatory submissions, and collaborate with teams to ensure project goals are met on time and within budget.
Coordinate and facilitate clinical trial activities, providing administrative and technical support to the project team. Manage study-specific documentation, perform file reviews, and act as a cross-functional liaison to ensure tasks are completed on time and within budget.
Manage and expand strategic relationships with key biopharmaceutical customers to drive revenue growth. Collaborate with cross-functional teams to align bioproduction portfolios with customer goals and ensure flawless execution.
Drive growth within health systems and laboratories by advancing the adoption of immunodiagnostic testing solutions. Orchestrate internal resources to expand testing menus and communicate clinical and economic value to senior executive stakeholders.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They act as a key country-level contact for regulatory activities and maintain accurate trial status information in tracking databases.
Perform on-site installation, alignment, and repair of sophisticated electron microscopy equipment for electronics research and manufacturing clients. Provide technical support, conduct planned maintenance, and collaborate with application scientists to resolve complex system issues.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They act as a key country-level contact for regulatory activities and maintain accurate trial status information in tracking databases.
Lead the North American commercial organization for BioProcessing to drive profitable revenue growth and market share. Develop and execute commercial strategies while managing sales operating rhythms and strengthening customer relationships.
The Clinical Data Team Lead manages data management activities for clinical trials, acting as the primary liaison between the client and the project team. Responsibilities include developing project documentation, monitoring study metrics, and mentoring junior staff to ensure operational excellence.
Accountable for achieving final clinical deliverables and clean data within contractual timelines and budgets. Manages operational and quality aspects of complex clinical studies in compliance with ICH GCP guidelines.
Perform on-site installation, planned maintenance, and repair of sophisticated electron microscopy equipment. Provide technical training to customers and collaborate with product quality teams to improve system documentation.
Develop and maintain direct customer relationships within the semiconductor and electronics sectors in Japan to drive sales growth. Responsibilities include creating strategic sales plans, conducting product demonstrations, and serving as a technical advisor for advanced analytical instruments.
Develop and manage the global Make/Buy strategy by designing analytical frameworks and validating site P&Ls. Lead cross-functional teams to identify cost efficiencies and optimize the manufacturing network through rigorous financial and operational analysis.
Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Identify safety trends, resolve complex issues, and support the creation of safety and medical management plans.
Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.
Lead the management and coordination of medical projects to ensure compliance and optimal performance throughout the project lifecycle. Perform safety data reviews, manage project financials, and serve as the primary point of contact for clinical project teams.
The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, alignment, and optimal performance throughout the project lifecycle. This includes reviewing safety data, managing project financials, and serving as the primary point of contact for clinical project teams.
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, adverse events, and clinical trial deliverables such as CSRs and periodic safety reports.
Lead the collection, organization, and analysis of qualitative data to build a best-in-class qualitative research center of excellence. Manage staff, vendors, and AI-enabled technologies while developing business plans and quality assurance processes for patient-centered research.
Provide comprehensive customer support and technical leadership for FIB-SEM systems to solve physical analysis challenges and improve semiconductor yield. Responsibilities include developing automation recipes, supporting sales through PoCs, and collaborating with product development teams.
The role involves preparing and finalizing global investigator grant budgets and payment schedules for multiple studies. It also requires coordinating with clients and internal teams to align budget negotiations with site activation timelines.
The Staff Technical Sourcing Engineer develops strategies for cost savings and risk mitigation while ensuring supplier quality for electrical and electro-mechanical components. This role involves collaborating with R&D and procurement to align global sourcing strategies and managing projects through their entire lifecycle.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They serve as the primary country contact for regulatory activities and maintain accurate trial status tracking in databases.
Drive business growth for Proteomic Sciences by spearheading sales engagements across academia, clinical research, and biopharmaceutical sectors. Focus on expanding the installed base, executing go-to-market strategies, and managing regional growth targets in the ANZ market.
Lead strategic development engagements to align customer needs with scientific capabilities and accelerate business growth. Coordinate integrated product development plans from preclinical to post-approval while managing stakeholder relationships and resource allocation.
Perform and coordinate clinical monitoring and site management to ensure trial conduct aligns with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The CRA is responsible for monitoring and managing clinical trial sites to ensure compliance with study protocols and regulatory requirements. This includes conducting on-site and remote visits, reviewing data for accuracy, and safeguarding patient safety.
The Assistant CRA performs remote activities to support site preparedness, monitoring processes, and site management in accordance with SOPs. Responsibilities include managing essential documents, coordinating study supplies, and performing data reconciliation tasks.
The Clinical Trial Manager is responsible for achieving final clinical deliverables and clean data within contractual timelines and budgets. This includes managing operational and quality aspects of studies, developing clinical tools, and leading clinical teams in compliance with ICH GCP.
Perform clinical monitoring and site management to ensure trial conduct aligns with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The role involves preparing and coordinating local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. It also includes managing trial status tracking, maintaining study files, and collaborating with internal departments and investigators.
The role involves monitoring investigator sites to ensure protocol and regulatory compliance using a risk-based approach. Responsibilities include conducting site visits, managing essential documentation, and facilitating communication between sites and sponsors.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring activities. Coordinate site management tasks, document collection, and system access in accordance with SOPs and regulatory guidelines.
Provide medical leadership and support for clinical trials, including the creation of protocols and real-time medical monitoring of study subjects. Serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and safety.
Perform periodic maintenance, troubleshooting, and installation of electron microscopes and X-ray photoelectron spectrometers. Collaborate with sales teams to plan equipment layouts and provide technical support to customers.
Perform periodic maintenance, troubleshooting, and installation of electron microscopes and analytical devices. Collaborate with sales teams to plan equipment layouts and specifications for customer sites.
Provides medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Responsible for medical review of safety data, serious adverse events, and the preparation of periodic safety reports.
Lead the drafting, negotiation, and finalization of clinical trial agreements and investigator budgets. Collaborate with sites, sponsors, and legal teams to ensure efficient site activation and risk mitigation.
Lead the operational delivery of clinical studies from start-up through closeout, ensuring quality, compliance, and adherence to timelines. Manage cross-functional teams, oversee Trial Master File quality, and maintain strong communication with sponsors and investigative sites.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting remote and on-site visits, managing essential documentation, and maintaining collaborative relationships with clinical sites.
Lead the design and implementation of robust bioanalytical strategies within a client-dedicated global biopharma team. Coordinate with lab-based scientists and regulatory agencies to mitigate risk and submit necessary documentation.
The Business Development Manager is responsible for developing and managing high-level relationships with academic and pharmaceutical customers to achieve sales objectives. This includes providing technical presentations, guiding study designs, and managing biomarker discovery projects to grow overall revenue.
Lead supplier quality activities including qualification, audit prioritization, and performance improvement to reduce nonconformances. Collaborate across functions to drive root-cause resolution and manage supplier corrective actions (SCAR).
The role supports supplier quality operations by partnering with procurement and engineering to resolve quality issues and conduct supplier evaluations. It involves monitoring supplier performance through KPIs and managing nonconformances to protect product quality.
Accountable for the end-to-end operational strategy, planning, and delivery of clinical studies to ensure they meet time, quality, and budget requirements. Leads the Study Leadership Team and manages FSO vendors while driving innovative approaches to study delivery.
Coordinate and review local regulatory submissions and site essential documents in alignment with global submission strategies. Partner with internal teams and CROs to track site activation metrics and ensure eTMF accuracy.
The Site Contract Specialist is responsible for drafting, negotiating, and finalizing clinical trial agreements and budgets with study sites. They collaborate with internal teams and CROs to ensure quality, objectivity, and timely delivery of contracts while adhering to fair market value guidance.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage strategic accounts and build executive-level relationships to position the company as a preferred provider.
Drive sales growth and customer success for advanced analytical instruments across diverse markets including pharmaceutical and environmental sectors. Manage the full sales cycle from identifying opportunities and providing quotations to negotiating contracts and maintaining account pipelines.
The Technical Sales Specialist is responsible for driving revenue growth of instrument and consumables portfolios within the Chromatography and Mass Spectrometry Division. This involves managing the full sales cycle from prospecting to closing while acting as a technical advisor to customers and account managers.
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, including serious adverse events and periodic safety reports across the product life-cycle.
Design and manage secure, scalable, multi-tenant database architectures for a healthcare SaaS platform. Ensure strict compliance with healthcare regulations like HIPAA and GDPR while optimizing performance for large-scale datasets.
The role involves providing medical science and strategy expertise to support RFPs, bid defenses, and the development of clinical trial protocols for metabolic diseases. The incumbent will also engage with senior pharmaceutical leadership and mentor internal clinical scientists to drive business growth.
The role involves providing medical science and strategy expertise to support oncology proposals, bid defenses, and clinical trial protocol design. It also requires engaging with senior pharmaceutical leadership and mentoring internal clinical scientists to drive business growth.
Manage the final quality of clinical and medical device translations to ensure regulatory compliance. Maintain language assets including translation memories, terminology, and style guides for Czech and Slovak.
Manage and coordinate local regulatory and ethical submissions to support clinical trial startup in alignment with global strategies. Act as the primary country-level contact for site activation and maintain accurate trial status tracking databases.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage strategic accounts and build executive-level relationships to position the company as a preferred provider.
Perform and coordinate all aspects of the clinical monitoring process independently. Provide end-to-end support for clinical trials from study start-up through to close-out.
Install, maintain, and repair sophisticated electron microscopy systems including SEM, TEM, and FIB instrumentation. Provide technical support to customers, conduct preventive maintenance, and ensure optimal system performance through complex troubleshooting.
The Regulatory Affairs Manager will lead the preparation of global clinical trial submissions and provide strategic regulatory guidance to internal and external clients. They are responsible for overseeing multiple projects, managing budgets, and ensuring high-quality regulatory performance across the clinical development lifecycle.
The Principal Regulatory Affairs Specialist will lead global regulatory strategies for clinical trials and act as a primary liaison with internal and external clients. They are responsible for coordinating regulatory submissions, managing project teams, and representing the department in client and regulatory agency meetings.
The Senior Sales Manager will lead the sales team to drive growth in the Materials Sciences Electron Microscopy business for Academia and Government sectors. Responsibilities include executing strategic sales plans, managing key accounts, and fostering relationships with opinion leaders to drive market creation and customer adoption.
The Process Instrument Sales Representative will lead all aspects of the sales process for Molecular Spectroscopy process instruments in a multi-state western region. Responsibilities include coordinating technical interactions, delivering product demonstrations, and meeting sales goals.
Provide medical leadership to study teams, including creating clinical trial protocols based on the latest scientific information and contributing to document review and approval. Perform real-time medical monitoring of clinical studies to ensure medical validity and subject safety, while identifying and escalating medical issues early.
The Clinical Research Associate (Level II) will conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure trials adhere to approved protocols, ICH-GCP guidelines, and SOPs. Key duties include monitoring investigator sites using a risk-based approach, performing data review, assessing investigational product, documenting observations, and escalating deficiencies to management.
This role involves ensuring high-quality input into significant requests for proposals, including strategy, regulatory issues, and protocol considerations for cardiovascular indications. The incumbent will also support proactive client engagement, develop product plans through consulting, provide therapeutic expertise to internal teams, and contribute to innovative initiatives.
Provide medical leadership to study teams and ensure the medical validity of clinical studies. Contribute to the creation and review of clinical trial protocols and ensure compliance with medical aspects.
The Principal CRA will lead and coordinate all aspects of clinical monitoring and site management for complex trials, ensuring adherence to protocols, ICH-GCP, and regulatory requirements while acting as a subject-matter expert and escalation point. Key duties involve leading monitoring activities, performing site visits, overseeing data review, managing essential documents, and driving corrective actions.
The Clinical Compliance Manager leads the assessment and classification of serious breaches in clinical trials and serves as the primary contact for breach investigations. This role also involves preparing notifications for regulatory authorities and developing standard operating procedures related to breach management.
The Senior Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management, ensuring compliance with protocols and regulations. They develop relationships with investigational sites and ensure audit readiness while documenting observations and resolving issues.
The Senior Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management, ensuring compliance with protocols and regulations. They develop relationships with investigational sites and manage documentation while conducting remote or on-site visits.
Achieve or exceed assigned territory sales plan while applying strong technical expertise in qPCR, dPCR, and sequencing. Develop and implement strategic account and territory plans to drive sales growth.
