The Technical Sales Specialist will support field sales activities and customer engagement across the downstream bioproduction workflow portfolio in Germany, the Netherlands, and V4 countries. They will collaborate with account managers and cross-functional teams to identify customer needs, provide technical expertise, and position Thermo Fisher Scientific's solutions.
The Import Export Coordinator executes import and export activities in compliance with company and client requirements. They also maintain documentation files and participate in department project teams to ensure regulatory standards are met.
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.
Manage end-to-end recruitment across multiple business functions while serving as a trusted advisor to hiring managers. Proactively source talent, build pipelines, and utilize recruiting metrics to drive effective hiring strategies.
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 requirements.
The Senior Site Contract Specialist manages the end-to-end preparation, negotiation, and finalization of investigator contracts. They ensure compliance with budgetary guidelines and contractual processes while identifying and mitigating legal, financial, and operational risks.
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 solve complex technical challenges.
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.
The Technical Project Lead is responsible for owning the technical delivery of laboratory informatics solutions, including design, architecture, and implementation. They act as a primary technical point of contact for customers and collaborate with internal teams to ensure projects are delivered on time and within budget.
The Clinical Trial Coordinator provides administrative and technical support to project teams while overseeing trial activities and documentation. They act as a cross-functional liaison, manage study-specific systems, and ensure compliance with regulatory standards and project timelines.
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 process improvements across clinical trials.
Supports clinical trial site preparedness and management, remote monitoring, study documentation, training, system access, vendor coordination, and site supply logistics under the direction of the CRA and study Clinical Lead. Performs assigned reconciliation and follow-up tasks, supports site payments and document compliance, and completes administrative duties such as expense reports and timesheets.
Lead and deliver complex pharmacometric analyses across clinical development, including model planning, development, evaluation, simulation, interpretation, and reporting. Provide scientific leadership through project coordination, senior review, client communication, mentoring, and improvement of pharmacometrics processes.
Lead North America go-to-market strategy and a multidisciplinary marketing organization to grow utilization, market share, revenue, and customer value across Allergy and Autoimmunity portfolios. Own regional portfolio and demand-generation plans, digital and customer experiences, sales enablement, marketing investment, analytics, commercialization readiness, and compliance.
Coordinates pharmacovigilance project activities, including review and tracking of safety data, committee meetings, contractual documents, training, and audit-ready project files. Acts as a subject matter expert, resolves complex support issues, improves processes, and mentors junior staff while supporting client and departmental needs.
Provide technical leadership and consulting to biotechnology and biopharmaceutical customers across downstream bioprocessing workflows, including demonstrations, process optimization, troubleshooting, training, and technology implementation. Collaborate with commercial and technical teams, document customer engagement, and share customer feedback to support product improvements and customer outcomes.
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 Global Clinical Integration Lead will provide strategic project and programme management support for complex business development, integration, and transition activities within Clinical Operations. They will coordinate cross-functional stakeholders, develop clear roadmaps, and ensure that high-priority initiatives are effectively planned and executed.
The Field Service Engineer is responsible for the installation, maintenance, and qualification of standardized scientific systems within the Freiburg region. They will perform routine repairs, document service activities, and provide technical support to customers while escalating complex issues to the appropriate teams.
The recruiter will manage the full recruitment lifecycle for high-volume positions, including sourcing, candidate engagement, and onboarding. They will collaborate with hiring managers and HR colleagues to build candidate networks while ensuring compliance with employment laws.
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.
Design, develop, and deliver technical sales learning programs to enhance commercial capability and sales productivity across the Asia Pacific, Japan, and Greater China regions. Collaborate with cross-functional teams to translate complex scientific concepts into engaging learning experiences while managing digital content and reporting on training metrics.
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.
The Senior Marketing Manager will lead the development and execution of integrated marketing strategies for biopharma workflows, positioning chromatography and mass spectrometry solutions. This role involves managing a high-performing team and collaborating across global functions to drive commercial growth and customer engagement.
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 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 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.
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 role involves performing standard customer service representative duties. The position operates on a standard Monday through Friday schedule.
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 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.
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.
The Associate Director/Director will lead global regulatory strategy and execution for late-stage development programs through marketing authorization. They will coordinate cross-functional submissions, manage health authority interactions, and ensure compliance across the product lifecycle.
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.
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.
Lead complex, enterprise-wide IT projects and programs, managing scope, schedules, budgets, and resources using traditional and agile methodologies. Collaborate with business stakeholders, vendors, and technical teams to deliver strategic technology solutions while meeting quality and regulatory requirements.
The Field Service Engineer is responsible for the installation, integration, maintenance, and troubleshooting of laboratory systems and associated software. They will provide timely technical support to customers, perform preventative maintenance, and ensure accurate service reporting.
Manage customer transactions and relationships, including orders, inquiries, complaints, delivery issues, claims, and payment discrepancies. Coordinate with internal teams, monitor work queues and service-level targets, escalate issues, and contribute to process improvements and customer service performance.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management, including document collection, system updates, and remote monitoring tasks. They coordinate study supply management and assist with site payments and reconciliation processes under the direction of the CRA.
The Senior Clinical Data Team Lead acts as the primary data manager for complex clinical projects, serving as a liaison between the client and the internal project team. They are responsible for overseeing study metrics, managing project budgets, and mentoring junior staff to ensure adherence to timelines and quality standards.
The Country Approval Specialist manages and coordinates local regulatory submissions and site start-up activities in alignment with global strategies. They provide regulatory advice, negotiate site budgets, and ensure all trial documentation is maintained according to SOPs.
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 site activation timelines and compliance standards are met.
The Senior Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also act as a study lead, facilitate cross-functional liaison, and support process improvement initiatives.
Lead complex, end-to-end finance transformation projects including cost accounting and ERP implementations across a global matrixed environment. Drive organizational change, manage project risks, and provide executive-level reporting to ensure alignment with company objectives.
Provide strategic leadership and oversight for the Medical Writing Functional Service Partnership portfolio to ensure operational excellence and business growth. Lead high-performing teams while building strong relationships with clients and cross-functional partners across the organization.
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 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 role involves leading clinical teams, developing monitoring plans, and maintaining compliance with ICH GCP and regulatory standards.
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 Principal Site Contract Specialist leads the negotiation and finalization of complex site contracts while ensuring compliance with budgetary and legal parameters. The role also involves mentoring junior staff, developing training plans, and coordinating with internal departments to ensure efficient site activation.
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 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 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 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.
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, and managing documentation to ensure audit readiness and subject well-being.
The Field Applications Scientist provides technical support, training, and product demonstrations to customers to optimize their scientific workflows. They collaborate with cross-functional teams including sales and R&D to drive business growth and ensure customer success.
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 to meet deliverables while ensuring compliance with regulatory requirements and internal SOPs.
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 Manager will oversee, coach, and mentor a clinical operations team while ensuring adherence to company SOPs and regulatory standards. They will also manage project metrics, facilitate training, and collaborate with leadership on resourcing and strategic business initiatives.
The Sales Development Associate qualifies inbound leads and engages prospective customers to identify new business opportunities. They support field sales teams by managing lead information in CRM systems and tracking biotech funding to drive account development.
The Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety variables, perform medical reviews of adverse events, and provide medical consultation to project teams and clients.
The Commercial Manager will drive sales growth and customer success for chromatography and mass spectrometry instruments by managing account relationships and collaborating with channel partners in Saudi Arabia. They will lead sales strategies, provide technical expertise, and coordinate with internal teams to meet or exceed sales objectives.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Conducts on-site and remote visits to assess regulatory adherence and manages essential trial documentation.
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 role involves providing statistical leadership for clinical trials, including study design, analysis, and reporting. You will collaborate with cross-functional teams and act as a project lead to ensure scientific rigor and regulatory compliance.
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 accountant will manage statutory reporting, audit processes, and tax compliance for various group entities. They will also coordinate with internal and external stakeholders to ensure accurate financial reporting and risk mitigation.
The Account Development Analyst supports RFP funnel growth by researching prospective clients, identifying leads, and nurturing relationships. They also manage marketing-generated leads, provide team training, and develop strategic plans to support sales volume.
Provide implementation, operational, and maintenance support for enterprise software applications and laboratory systems. Resolve application issues, execute change requests, and maintain system documentation to ensure optimal performance.
Develop and execute strategic territory account plans to drive growth across allergy and autoimmunity portfolios while managing the full sales cycle. Build trusted relationships with key decision-makers in healthcare and laboratories to improve patient pathways and achieve sales targets.
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 resolve complex safety-related issues.
The Global Product Manager will drive brand differentiation and awareness strategies for B·R·A·H·M·S PCT by translating clinical and health-economic data into compelling value propositions. They will collaborate with cross-functional teams to develop marketing content, educational initiatives, and strategic communication tools to support global biomarker adoption.
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.
You will be responsible for prospecting within an assigned territory to uncover new business opportunities and directing leads into the appropriate conversion path. You will also collaborate closely with field sales and marketing teams to drive business growth and accelerate the adoption of Olink proteomics solutions.
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 Sales Specialist will drive growth for the Olink Proteomics portfolio by identifying new business opportunities and managing relationships across academia, biotech, and pharma sectors. The role requires significant field time to engage with researchers and key opinion leaders to align proteomics solutions with their scientific research needs.
Performs and coordinates all aspects of the clinical monitoring and site management process to ensure protocol and regulatory compliance. Acts as a site processes specialist to guarantee subject rights, well-being, and data reliability while maintaining audit readiness.
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 role involves performing and coordinating clinical monitoring and site management processes to ensure protocol and regulatory compliance. Responsibilities include conducting remote or on-site visits, managing documentation, and ensuring data reliability through risk-based monitoring.
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 documentation to ensure audit readiness.
The Start-up Team Manager oversees site activation activities, ensuring compliance with regulatory standards and project timelines across assigned regions. They facilitate collaboration between internal teams and trial sites while managing technical, operational, and risk-mitigation aspects of clinical studies.
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.
You will develop and manage 24-month demand plans for key product portfolios while facilitating Sales & Operations Planning (S&OP) processes. Additionally, you will collaborate with cross-functional teams to enhance forecast accuracy, optimize inventory levels, and implement continuous improvement initiatives.
Provide technical expertise and support for LC-MS instrumentation to customers, focusing on small molecule quantitation and application optimization. Collaborate with cross-functional teams including sales, marketing, and R&D to drive customer success and business growth.
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 FSP Manager Clinical Operations oversees, trains, and mentors a team of clinical staff while ensuring adherence to SOPs and project metrics. They also collaborate with leadership on resourcing, process improvement, and strategic business development initiatives.
Lead the strategy, requirements, and delivery of innovative AI solutions within the HR department. Partner with stakeholders and engineering teams to define use cases, manage project lifecycles, and drive the adoption of AI technologies.
The Manager of Clinical Operations oversees, trains, and mentors a team while managing performance through metrics and key performance indicators. They also collaborate with leadership on resourcing, ensure adherence to regulatory standards, and facilitate process improvements.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of cross-functional projects in terms of quality, time, and cost. They are responsible for driving risk identification, issue resolution, and ensuring team compliance with organizational policies and regulatory requirements.
The Business Development Associate will review, qualify, and prioritize inbound leads while supporting field sales teams with prospecting and account development. They will also maintain accurate data in CRM systems and track biotech funding events to identify new sales opportunities.
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 Clinical Trial Coordinator provides administrative and technical support to project teams while facilitating project activities across global clinical trials. They are responsible for maintaining study documentation, ensuring compliance with regulatory standards, and managing project-specific trackers and systems.
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.
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They are responsible for site initiation, ongoing monitoring, issue resolution, and trial close-out activities while maintaining effective communication with investigative sites.
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 ensuring compliance, managing project budgets, and maintaining effective client interfaces throughout the product development lifecycle.
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 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 standards.
The Operational Bidding Specialist prepares and delivers competitive, high-quality operational bids and proposals for regulatory and medical writing services. They collaborate with internal teams to define bid strategies, labor requirements, and budget assumptions while ensuring alignment with client specifications.
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, and resources while ensuring high-quality deliverables and resolving client management issues.
The Senior Safety Specialist performs and oversees day-to-day pharmacovigilance activities, including the collection, monitoring, and evaluation of safety information. They also collaborate with project teams and stakeholders to ensure operational excellence and regulatory compliance across clinical trials.
The Senior Safety Reporting Specialist will lead the preparation and submission of complex safety reports while ensuring compliance with international pharmacovigilance regulations. They will also manage large-scale projects, provide guidance to team members, and contribute to the development of departmental procedural documents.
The Country Approval Specialist prepares, reviews, and coordinates local regulatory submissions while providing strategic advice to internal clients. They also manage site start-up activities and ensure all submission processes align with global strategic goals and timelines.
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 Trial Coordinator provides administrative and technical support to project teams while 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 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.
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 collaborate with cross-functional teams to meet customer needs.
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 Account Manager will drive revenue growth by developing strategic customer relationships and promoting a portfolio of scientific products. They are responsible for implementing sales strategies, identifying new business opportunities, and providing expert support to customers.
You will drive revenue growth by developing and maintaining strategic customer relationships while promoting a portfolio of scientific products. Additionally, you will implement sales strategies, identify new business opportunities, and provide support to help customers achieve their scientific goals.
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 study metrics while ensuring compliance with regulatory guidelines and SOPs.
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 manage and develop high-level customer relationships within academia, pharma, and biotech sectors to drive sales of Olink proteomics products. The role involves implementing strategic sales plans and providing consultative solutions to meet customer research needs.
Design, develop, and validate AI/ML and NLP solutions to support safety operations and pharmacovigilance data management. Serve as a technical lead for the Oracle Argus Safety system while ensuring compliance with global regulatory standards.
You will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Additionally, you will serve as a trusted advisor to customers, providing tailored scientific solutions through both virtual engagement and site visits.
Develop and implement strategic sales plans to achieve revenue and margin objectives within the assigned territory. Build and maintain robust customer relationships while promoting the company's portfolio of scientific products and services.
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.
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.
You will coordinate all aspects of clinical monitoring and site management to ensure trials are conducted according to protocols and regulatory standards. This includes performing remote or on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
Perform on-site installation, maintenance, and repair of sophisticated electron microscopy equipment. Provide technical training to customers and maintain positive relationships while documenting service activities.
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 Senior Validation Specialist will implement, configure, and support LIMS products while managing computer system validation activities. They will lead validation projects, ensure compliance with GxP/GLP standards, and collaborate with cross-functional teams to translate laboratory requirements into validated solutions.
The Field Service Engineer is responsible for the installation, maintenance, troubleshooting, and repair of sophisticated analytical and scientific instruments. They will provide exceptional customer service while supporting research, industrial, and healthcare clients.
The Pharmacovigilance Physician provides medical oversight for pharmacovigilance activities, ensuring compliance with regulatory requirements and company SOPs. They perform medical review and analysis of serious adverse events, signal detection, and contribute to the management of product benefit-risk profiles.
The Sales Development Representative II will identify and develop new business opportunities while nurturing customer relationships across a scientific portfolio. They will collaborate with cross-functional teams to provide innovative solutions that help customers advance their research and healthcare outcomes.
The Business Development Associate is responsible for qualifying inbound leads, engaging prospective customers, and routing opportunities to field sales representatives. They also support sales teams with prospecting, account development, and maintaining accurate data within the CRM system.
The Regulatory Affairs Specialist is responsible for reviewing and approving country- and site-level essential documents to ensure compliance and support timely site activation. They also maintain knowledge of regulatory guidelines and track review details within the company's data tracking systems.
Lead global sales enablement, commercial operations, and AI-driven transformation to drive revenue growth and sales productivity. Partner with leadership to design sales strategies, training programs, and analytics dashboards to improve commercial effectiveness.
The Field Service Engineer will provide installation, maintenance, troubleshooting, and repair services for Phadia ImmunoDiagnostics systems at customer sites. They will manage their own field-based workload while collaborating with technical support, sales, and other colleagues to ensure optimal instrument performance.
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 Project Manager will lead and coordinate central laboratory activities across clinical trial programs, serving as the primary liaison between internal teams and external clients. Responsibilities include managing study timelines, budgets, risk assessments, and ensuring high-quality data delivery throughout the study lifecycle.
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 Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage documentation, and facilitate communication between investigative sites and project teams.
The Medical Writer is responsible for planning, coordinating, and authoring 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 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 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.
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.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include maintaining essential documents, coordinating site supplies, and assisting with study-specific system updates and data reconciliation.
The Field Service Engineer is responsible for the installation, maintenance, troubleshooting, and repair of laboratory instruments within an assigned territory. They must build strong customer relationships while ensuring service objectives and documentation requirements are met.
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 Field Service Engineer will assemble, install, calibrate, and maintain electromechanical instrumentation while ensuring high-quality service and customer satisfaction. The role involves conducting root cause analysis, performing preventative maintenance, and managing administrative service records.
The Senior Technical Sales Specialist will drive revenue growth by identifying new opportunities and managing a sales funnel for single-use technologies. They will collaborate with account managers and field application scientists to develop account strategies and provide technical expertise to customers.
Lead client programs within the regulatory medical writing team by managing project timelines, budgets, and client relationships. Ensure operational excellence and high-quality document delivery while serving as a subject matter expert and mentor to junior staff.
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 Safety Writer III is responsible for planning, coordinating, and delivering safety writing services for clinical trials and marketed products within a regulated pharmacovigilance environment. This role involves leading project teams, conducting data reviews, and ensuring all deliverables comply with regulatory standards and internal policies.
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.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They facilitate communication between sites and project teams while managing essential documentation and trial status reporting.
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 Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and sponsors.
Manage and coordinate clinical monitoring and site management activities to ensure trials comply with protocols, ICH-GCP, and regulatory standards. Perform remote and on-site monitoring, including source data verification and site deficiency resolution, to maintain data quality and patient safety.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
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 Senior Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol and regulatory compliance. They conduct remote or on-site visits to assess data accuracy, manage site documentation, and facilitate effective communication between investigative sites and the project team.
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.
The 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, oversee project financials, and ensure compliance with ICH GCP and regulatory standards throughout the study lifecycle.
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 Clinical Trial Coordinator II provides administrative and technical support to the project team, ensuring audit readiness and efficient site activation. They are responsible for performing file reviews, managing study metrics, and maintaining accurate trial status information in accordance with SOPs.
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 maintaining collaborative relationships with investigational sites.
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, develop study tools, and ensure compliance with ICH GCP and regulatory standards throughout the trial lifecycle.
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 Regional Sales Manager will support sales growth and customer success for advanced analytical and scientific instruments across diverse markets. They are responsible for developing and expanding customer relationships while executing strategic sales plans to meet business objectives.
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.
Lead and mentor a team of application scientists to provide high-quality technical support and consultative services for proteomics workflows. Collaborate with sales teams to drive market presence while ensuring customer satisfaction through effective demonstrations and troubleshooting.
The Director of Sales will lead the EMEA Human Identification commercial strategy to drive sustainable growth and profitability. They are responsible for managing regional sales objectives, developing strategic customer relationships, and building a high-performing commercial team.
The HGRAC CAS is responsible for managing all Human Genetic Resource Administration of China (HGRAC) applications for clinical studies and supporting genetic resource management during trial implementation. This role involves preparing and reviewing application documents, tracking submission statuses, and maintaining databases of regulatory requirements and lessons learned.
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.
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 while maintaining accurate and verifiable study data.
Perform onsite installation, preventive maintenance, troubleshooting, and repair of chromatography instruments such as IC and HPLC. Manage territory activities, provide technical training to customers, and document all service activities accurately.
The Business Development Executive will drive sales growth by managing biotech accounts and identifying new opportunities within an assigned territory. They are responsible for executing territory plans, managing the sales pipeline, and collaborating cross-functionally to deliver integrated solutions to customers.
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.
The Senior Account Manager will manage key client relationships, drive revenue growth, and oversee project execution while ensuring high customer satisfaction. Additionally, the role involves providing leadership, coaching, and talent development to a team of account managers to support business objectives.
The Senior Clinical Trial Coordinator provides administrative and technical support to project teams while overseeing assigned clinical trial activities. They act as a cross-functional liaison, manage study documentation, and ensure project tasks are completed on time and within budget.
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.
The Field Service Engineer will perform installation, maintenance, and repair of sophisticated analytical and microscopy equipment at customer sites. They are responsible for resolving complex technical issues, conducting preventive maintenance, and providing user training to ensure optimal system performance.
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 Associate Director leads the innovation landscape by translating strategic priorities into validated discovery themes and actionable opportunities. They oversee a portfolio of projects, ensuring rigorous evidence-based decision-making and cross-functional alignment across digital, data, and scientific teams.
The Innovation Director drives innovation across the organization by shaping and overseeing a portfolio of high-impact opportunities aligned with strategic business priorities. They act as a senior interface between innovation teams and execution teams to ensure strategic intent is maintained throughout the validation and transition processes.
Lead a global team in managing sales compensation administration, incentive plan design, and territory alignment to drive commercial performance. Partner with cross-functional teams including Finance and Sales Operations to implement scalable solutions and provide data-driven strategic insights.
Perform installation, maintenance, and repair of sophisticated analytical and microscopy equipment at customer sites. Provide expert technical support, train users, and manage territory activities to ensure optimal system performance and customer satisfaction.
Lead a team of project managers and support staff while acting as a strategic partner to pharmaceutical and biotech clients throughout their clinical trials. Oversee complex global clinical supply chain operations, portfolio management, and financial performance to ensure high-quality service delivery.
The Director provides enterprise-level leadership across multiple strategic FSP accounts, driving portfolio strategy, operational transformation, and client partnership growth. They act as a strategic advisor to internal and external leadership to influence long-term delivery models and organizational performance.
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.
The FSP Recruiter will manage full-cycle recruitment for diverse roles across North America while serving as a strategic talent advisor. They will collaborate with hiring managers and HR teams to develop effective sourcing strategies and build strong talent pipelines.
The specialist will provide subject matter expertise on chemical regulations, manage registrations, and oversee compliance reporting for the Lithuania site. They will also lead cross-functional projects, develop training programs, and maintain internal tools to ensure adherence to global chemical control frameworks.
The Associate Medical Writer assists in researching, writing, and editing clinical and scientific documents such as informed consent forms and lay summaries. They also collaborate with internal and external clients to ensure operational excellence and compliance with quality standards throughout the document lifecycle.
Perform on-site installation, preventive maintenance, and repair of chromatography and mass spectrometry equipment. Provide technical training to customers and maintain accurate service documentation and reports.
The Senior Account Manager will drive revenue growth by managing strategic customer relationships and providing consultative sales for scientific products. They will collaborate with technical and support teams to deliver integrated automation solutions that advance critical research and manufacturing initiatives.
Provides nutrition expertise and operational support for clinical trial nutrition programs, including menu development and lifestyle interventions. Collaborates with internal teams and stakeholders to ensure regulatory compliance and high-quality execution of study requirements.
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.
Draft, review, and negotiate site agreements and investigator grant budgets while ensuring compliance with company and client standards. Coordinate with internal teams to align site startup activities and meet target cycle times for site activations.
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.
The Local Clinical Trial Manager leads the local study team and serves as the operational point-of-contact to ensure clinical deliverables meet time, budget, and quality expectations. They are responsible for managing study sites, regulatory submissions, vendor oversight, and ensuring compliance with GCP/ICH guidelines.
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 Clinical Sales Specialist will develop and implement strategic sales plans to drive growth within healthcare segments while managing key account relationships. They will provide consultative support to physicians and laboratory staff to ensure the effective adoption and utilization of diagnostic testing solutions.
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 audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
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 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 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.
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 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 Senior 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 risk assessments.
The Associate Clinical Data Team Lead assists with study setup, data cleaning, and database close-out tasks while supporting the lead data manager. They also coordinate data cleaning activities, monitor study metrics, and provide training to junior team members.
The Trial Delivery Specialist will manage end-to-end clinical study operations, including vendor oversight, eTMF maintenance, and project planning. They will partner with global study leaders to ensure inspection readiness, budget compliance, and the successful delivery of clinical trials.
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.
You will perform and coordinate clinical monitoring and site management activities to ensure trials adhere to protocols, ICH-GCP, and regulatory standards. This involves conducting on-site and remote monitoring, performing data verification, and maintaining clear communication with investigational sites.
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 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 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 Senior Staff Business Manager will drive business growth and strengthen strategic client relationships within the biologics drug substance business. They will lead commercial contracting, manage financial performance, and collaborate across internal functions to deliver coordinated solutions for customers.
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 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 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 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 manager will lead a team of project management staff to ensure the successful execution of laboratory projects and operational excellence. They will serve as the primary liaison between sponsors and internal departments while managing client relationships and procedural compliance.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements and investigator grant budgets. They also coordinate with internal teams to ensure site startup activities align with contractual timelines and risk management protocols.
The Manager Clinical Operations oversees, trains, and coaches a team while managing performance through metrics and key performance indicators. They also collaborate with leadership on resourcing, ensure adherence to regulatory standards, and support project deliverables.
Develop and execute strategic territory account plans to drive growth in allergy and autoimmunity portfolios while managing distributor performance in the Baltic region. Collaborate with internal stakeholders and key opinion leaders to influence patient pathways and increase diagnostic test volume.
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.
The National Account Executive will drive revenue growth and implement commercial strategies within top national laboratory accounts. They are responsible for fostering key relationships, managing contract compliance, and identifying new sales opportunities for immunoassay and protein diagnostic products.
The Advanced Application Specialist will optimize bioprocess workflows and drive technology adoption by providing expert consultative support to customers. They will act as a technical advisor throughout the process development and manufacturing lifecycle while collaborating with internal teams to shape product strategy.
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 manager will oversee a team to deliver high-quality feasibility assessments for clinical trials while managing project budgets and timelines. They are responsible for resource allocation, staff development, and ensuring cross-functional collaboration across global teams.
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 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 essential documentation in accordance with ICH-GCP guidelines.
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.
Install, maintain, and repair a diverse range of high-value analytical instruments to ensure peak performance. Deliver exceptional technical service while building strong relationships with customers in the field.
The Regulatory Affairs Scientist supports the development and execution of global and regional regulatory strategies for clinical programs. They contribute to the compilation of regulatory submissions and collaborate with cross-functional teams to manage Health Authority interactions and regulatory risks.
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.
The Field Service Engineer is responsible for the installation, maintenance, troubleshooting, and repair of mass spectrometry and trace elemental analysis equipment. They will also provide technical training to customers and support the sales of service contracts and upgrades.
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 Account Manager will develop and implement strategic sales plans to increase revenue while managing key account relationships. They will provide tailored scientific solutions to customers through a combination of virtual engagement and in-person visits.
The Service Sales Account Manager is responsible for meeting or exceeding sales plans by developing and executing territory plans to grow service contract revenue. They will proactively uncover new opportunities through outbound communication and cross-functional collaboration to drive business growth within the Life Sciences segment.
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 Senior Government Technical Proposal Writer leads the development of complex technical narratives for U.S. Government proposals, ensuring compliance with solicitation requirements and evaluation criteria. They facilitate engagement with subject matter experts to translate technical concepts into persuasive content while conducting market research and utilizing AI tools to enhance proposal quality.
The Regional Director provides strategic engineering leadership to ensure capability, capital investment, and operational excellence across the clinical trials division. They are responsible for developing regional engineering strategies, managing capital portfolios, and building high-performing teams to support business growth and regulatory compliance.
You will coordinate clinical monitoring and site management processes to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting remote or on-site visits, performing data reviews, and managing site compliance through effective problem-solving and communication.
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 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 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 Senior Director leads a regional team to drive revenue growth, customer retention, and strategic engagement within the biotech sector. They are responsible for executing commercial strategies, fostering high-performing teams, and building executive-level relationships with key stakeholders.
The Account Manager II 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 excellent support to help customers achieve their goals.
The specialist will build and cultivate relationships with physicians, healthcare professionals, and community leaders to drive clinical trial recruitment. They will travel regionally to conduct outreach, attend community events, and manage a network to support enrollment goals.
The Recruitment Strategy Manager will lead the development and execution of strategic participant recruitment campaigns to meet clinical study enrollment goals. They will serve as a subject matter expert, integrating data, marketing insights, and cross-functional collaboration to optimize recruitment performance and budget efficiency.
The Product Marketing Manager will lead the strategic direction and go-to-market execution for assigned products to drive profitable growth. This role involves collaborating with cross-functional teams to define product positioning, create demand generation programs, and ensure successful product launches.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within quality standards. They manage study documentation, track project metrics, and act as a liaison between cross-functional teams and clinical sites.
The Regulatory Program Manager will partner with Global Regulatory Leads to develop and execute comprehensive regulatory strategies across all stages of product development. This role involves facilitating cross-functional subteam meetings, managing complex timelines, and ensuring alignment on regulatory deliverables and milestones.
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 Clinical Trial Coordinator provides administrative and technical support to project teams by overseeing trial activities, maintaining study documentation, and ensuring compliance with quality standards. They also act as a cross-functional liaison, facilitate project activities, and support process improvements within the department.
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 Sample Coordinator performs various sample handling tasks including receipt, login, labeling, and inventory management in support of laboratory operations. They also communicate sample status to staff, ensure SOP compliance, and assist with investigation and deviation documentation.
The Country Approval Associate supports the preparation, review, and coordination of country submissions in alignment with global strategies. They also coordinate with internal departments to ensure site start-up activities and submission timelines are met.
The role involves providing end-user support for HR systems, resolving technical inquiries, and ensuring data integrity through audits and mass data loads. Additionally, the associate will collaborate with cross-functional teams to implement process improvements and maintain accurate system documentation.
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.
Manage bioanalytical operations for pre-clinical and clinical trials by coordinating activities across internal and external stakeholders. Ensure the timely delivery of high-quality data while overseeing vendor contracts and regulatory documentation.
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.
Drive business growth for Proteomic Sciences in Korea by identifying and converting sales opportunities across academic, pharmaceutical, and clinical sectors. Provide technical expertise and build strategic relationships with key customers to position the company as a trusted scientific partner.
You will manage key account relationships and implement strategic sales plans to increase revenue for scientific products. The role involves providing tailored solutions through consultative selling and serving as a trusted advisor to help customers achieve their scientific goals.
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.
The Field Service Engineer will travel to customer sites across the EMEA region to install, service, and repair bioproduction hardware and automation products. They will provide expert technical support, conduct equipment qualification protocols, and maintain strong customer relationships.
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.
Drive revenue growth and market share for protein expression solutions through technical sales excellence and product demonstrations. Partner with cross-functional teams to develop sales strategies and provide tailored solutions to meet customer needs.
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 Account Manager III will develop and implement strategic sales plans to increase revenue and build lasting customer relationships. They will serve as a trusted advisor by providing tailored scientific solutions through both virtual engagement and customer visits.
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 Project Manager is responsible for the overall delivery of clinical trials, ensuring quality, time, and cost objectives are met. They lead cross-functional teams, manage customer expectations, and oversee vendor performance while ensuring compliance with regulatory standards.
The specialist will drive revenue growth by identifying new client opportunities and providing technical leadership for complex scientific product portfolios. They will act as a trusted advisor to customers while collaborating with internal teams to execute sales strategies and support product adoption.
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.
The Local Clinical Trial Manager is responsible for leading local study teams and ensuring clinical deliverables meet time, budget, and quality expectations. They serve as the operational point-of-contact, managing site selection, regulatory submissions, and vendor oversight to ensure study integrity.
The Pricing Analyst will lead pricing processes and develop data analytics to measure business performance and pricing effectiveness. They will identify trends and provide actionable insights to support strategic business decisions across the organization.
Responsible for the installation, maintenance, and repair of genetic analysis systems in customer laboratories. Provides technical support, user training, and ensures compliance with quality standards and documentation requirements.
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 Senior Compliance Specialist manages GxP regulatory authority inspections across the EMEA region, providing consultation on inspection readiness and preparation. They also support project teams in investigating non-conformances, developing CAPAs, and facilitating post-inspection follow-up activities.
The Proposal Specialist creates and reviews compelling proposals and responses to client requests for information (RFIs) to position the organization as the optimal choice. They also liaise with subject matter experts to gather content and maintain strategic library resources for future use.
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 Site Payments Associate II is responsible for managing the reconciliation of investigator payments and ensuring strict adherence to contractual guidelines and regulations. They will compile data from multiple sources, resolve payment-related issues, and maintain strong relationships with study sites and teams.
The Site Payments Associate provides administrative support by tracking and managing investigator fee invoices throughout the payment process. They are also responsible for producing management metrics, maintaining trackers, and initiating workflows within the clinical research systems.
The Country Approval Specialist coordinates and prepares local regulatory submissions in alignment with global strategies. They also act as a key contact for regulatory activities and ensure site start-up processes align with project timelines.
The Senior Manager will oversee, coach, and manage a clinical operations team while ensuring adherence to SOPs and performance metrics. They will also collaborate with leadership on resourcing, business development, and quality assurance to support successful clinical trial delivery.
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 Account Executive will manage and grow revenue for the Protein Diagnostic Division by prospecting new laboratory and health system business while maintaining existing accounts. They will implement strategic sales plans, conduct instrument demonstrations, and act as a trusted advisor to customers to ensure long-term growth and satisfaction.
The Principal Operations Strategy Specialist provides expert guidance in the formulation and execution of clinical trial strategies to ensure operational efficiency and strategic alignment. They collaborate with cross-functional teams to develop budgets, manage proposal deliverables, and drive initiatives that enhance clinical trial success.
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 Clinical Sales Specialist is responsible for driving revenue growth through new business development and managing existing accounts within a specified territory. This role involves executing the full sales cycle, from lead qualification and cold calling to price negotiation and sales forecasting.
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 Inside Sales Representative is responsible for identifying new business opportunities and managing the existing customer base within Germany. They will position product and service solutions, manage contracts, and maintain sales pipelines in Salesforce to drive revenue growth.
The Business Development Executive will drive sales growth by executing territory plans and managing biotech accounts across various drug modalities. They are responsible for implementing business strategies, forecasting, and building trusted relationships with key stakeholders to secure new opportunities.
The Associate Contract Manager leads the review, negotiation, and finalization of contract templates and parameters while ensuring quality and risk assessment. They act as a regional interface for clients and collaborate with internal departments to facilitate site startup activities.
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.
The Technical Sales Specialist is responsible for driving revenue growth for inorganic spectroscopy 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 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 technical support to help customers achieve their goals.
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.
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 to ensure project compliance with regulatory requirements and drive effective risk identification and issue resolution.
The Field Service Supervisor leads, mentors, and develops a team of field service engineers while overseeing daily service operations and complex system repairs. They are responsible for maintaining strong customer relationships, ensuring regulatory compliance, and driving service delivery performance metrics.
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 Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management, including remote monitoring and document collection. They assist with study start-up, site preparedness, and the maintenance of study-specific systems and vendor trackers.
The Local 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 Compliance Manager is responsible for managing GxP audits and regulatory inspections across the APAC region for the company and its clients. They provide consultation on inspection readiness, lead audit reporting, and support project teams in developing CAPAs to address non-conformances.
The Business Development Manager will drive growth across academia, clinical research, and biopharmaceutical sectors by developing strategic customer relationships. They are responsible for managing the sales funnel, achieving revenue targets, and delivering innovative proteomics solutions.
The Country Approval Specialist manages and coordinates local regulatory submissions for clinical trials in alignment with global strategies. They also provide regulatory advice, support site start-up activities, and maintain accurate trial status information in tracking databases.
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 SOPs.
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.
The Sales Specialist will develop and implement sales strategies to drive growth for analytical instruments across a multi-state territory. They will manage customer relationships, perform sales calls, and collaborate with cross-functional teams to meet market needs.
The Project Manager will lead strategic functional initiatives and optimize operational workflows within the Global Patient Safety organization. They are responsible for managing project plans, facilitating governance meetings, and ensuring high-quality service delivery across global teams.
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 role involves providing technical and strategic leadership for CMC analytical development, including oversight of outsourced QC testing and regulatory compliance. You will manage change controls, deviations, and stability programs while contributing to global submission plans and product life cycle management.
Perform on-site installations, validations, preventive maintenance, and repairs of laboratory equipment while providing responsive technical support. Coordinate service schedules and deliver an outstanding customer experience to ensure instrument performance and customer satisfaction.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs and availability for clinical projects. They also coordinate project team compositions and liaise with internal departments to ensure efficient labor utilization and financial performance.
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.
The Regional Service Specialist provides advanced technical support, installations, and repairs for LC/MS instrumentation across the West Coast region. They also act as a technical resource to mentor Field Service Engineers and ensure high levels of customer satisfaction and service performance.
The Account Manager II supports a key pharmaceutical customer by executing account strategies and identifying new business opportunities. This role involves collaborating with internal stakeholders to deliver a consistent customer experience and managing defined customer relationships.
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, manage documentation, and resolve site-level issues.
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.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs and availability for clinical projects. They also coordinate project team compositions and liaise with internal departments to prioritize resourcing for future work and bid defense meetings.
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.
The Senior Key Account Manager will lead commercial strategy and business development for global pharmaceutical accounts, driving revenue growth for proteomics and biomarker discovery solutions. This role acts as a central orchestrator across matrixed teams to ensure coordinated engagement and successful execution of strategic account plans.
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 Account Manager will develop and maintain strategic relationships with customers in the London, Ontario area to drive revenue growth. They will implement sales strategies, identify new business opportunities, and provide expert support for a portfolio of scientific products.
The specialist will draft, review, and negotiate clinical trial site contracts, budgets, and amendments while ensuring compliance with internal processes. They will also coordinate with internal functional teams to ensure site startup activities align with contractual timelines and target cycle times.
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 Senior Technical Sales Specialist will manage and grow the sales funnel for single-use technologies within the BioProduction Group. This role involves collaborating with account managers and field application scientists to develop account strategies and drive new product adoption.
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 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.
The Safety Physician provides medical and operational oversight for end-to-end pharmacovigilance activities, including ICSR medical assessment and coding standards. They also lead quality control initiatives, support benefit-risk strategies, and act as a primary point of contact for cross-functional medical review requirements.
The EDP reviewer is responsible for the review and approval of country and site essential documents to ensure completeness, accuracy, and quality. They also track review details in data systems and communicate deficiencies to the EDP submitter.
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 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, managing project financials, and ensuring compliance with ICH GCP and regulatory standards.
The Senior Demand and Supply Manager leads the design and implementation of inventory management plans for complex clinical trials to ensure continuous supply. They also act as an informal leader, providing mentorship to the team and managing financial forecasts and IRT strategy.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of cross-functional projects in terms of quality, time, and cost. They are responsible for managing customer expectations, driving risk identification, and ensuring compliance with regulatory requirements and internal SOPs.
The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.
The Accountant II will perform monthly closing activities, including journal entries and financial analysis, while ensuring compliance with U.S. GAAP and Sarbanes-Oxley requirements. They will also drive continuous improvement in financial systems and support internal and external audit processes.
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 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 essential documentation in accordance with ICH-GCP guidelines.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence. They will manage site processes, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial lifecycle.
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 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 Senior Account Director is responsible for securing and retaining business by positioning the company as a preferred provider of medical communication services to biopharma and biotech sponsors. This role involves orchestrating RFP strategies, negotiating contracts, and acting as a primary liaison between clients and internal teams to ensure successful project implementation.
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 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 Regulatory Liaison acts as the primary interface for clinical trial teams, ensuring compliance with global and local regulations. They are responsible for preparing, reviewing, and coordinating regulatory submission packages while maintaining transparency throughout the trial lifecycle.
The Clinical Demand Specialist will manage account profiling and develop relationships with key healthcare stakeholders to drive PCT testing strategies. They will also deliver educational programs and execute business growth plans to support clinical adoption of diagnostic protocols.
The Portfolio Associate supports cross-functional PMO operations by maintaining portfolio data, coordinating project documentation, and ensuring the accuracy of management tools. This role assists with reporting cycles, data validation, and process improvements while working closely with project managers and stakeholders.
The Account Executive is responsible for securing revenue objectives for oncology and special protein products by prospecting new business and maintaining existing accounts. They will develop sales strategies, conduct instrument demonstrations, and manage contract renewals while collaborating with cross-functional teams to ensure customer success.
The specialist will perform daily pharmacovigilance activities including the collection, assessment, and tracking of safety information. They will also collaborate with project teams and regulatory bodies to ensure compliance and accurate reporting of adverse events.
Lead and perform complex internal and external GCP audits to ensure compliance with regulatory standards and client requirements. Prepare comprehensive audit reports and provide quality support to project teams and external clients.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global submission strategies. They act as the key contact for regulatory activities and ensure site start-up processes meet established timelines.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial agreements and investigator grant budgets with study sites. They must ensure compliance with internal processes, manage financial and operational risks, and coordinate with internal teams to meet site activation timelines.
You will manage supplier qualification processes, conduct comprehensive audits, and implement continuous improvement initiatives to ensure supply chain quality. Additionally, you will collaborate with cross-functional teams to resolve quality issues and maintain compliance with industry standards and regulations.
The Associate Safety Administrator coordinates safety documentation, manages protocol inquiries, and tracks adverse events for clinical trials. They also facilitate project meetings, perform data entry, and ensure compliance with regulatory standards and internal SOPs.
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 Laboratory Consumables Representative is responsible for meeting and exceeding sales forecasts within a designated geographic territory by pursuing new business and maintaining strong client relationships. They will also collaborate with channel partners and internal teams to promote the company's full breadth of product offerings.
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, troubleshoot, and repair analytical instrumentation including Chromatography and Mass Spectrometry systems. They are responsible for delivering exceptional technical support while building trusted relationships with customers across various laboratory environments.
Manage study-level site payment activities and ensure project milestones, quality standards, and contractual deliverables are achieved. Act as the functional lead for assigned studies by monitoring financial health and serving as the primary contact for key stakeholders.
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 Account Manager will partner with scientists to represent a portfolio of laboratory products and services while executing sales strategies. They are responsible for building strong customer relationships, identifying growth opportunities, and delivering innovative scientific solutions.
The Field Service Engineer is responsible for the installation, repair, maintenance, and validation of clinical instruments including Microarray, PCR, and qPCR platforms. They must provide on-site and telephone support to ensure customer satisfaction while managing company assets and reporting activities accurately.
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 role involves managing contract lifecycles, including drafting, reviewing, and negotiating commercial agreements while ensuring regulatory compliance. Additionally, the specialist will oversee tender management processes, monitor public databases, and coordinate with internal departments to ensure timely submission of documentation.
The Product Specialist II will provide technical sales expertise and guidance to customers across academic, pharmaceutical, and biotech sectors. They are responsible for conducting product demonstrations, managing customer relationships, and delivering value propositions to support research and manufacturing goals.
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 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 execute product launches, optimize portfolio performance, and ensure alignment with market needs and commercial objectives.
The Clinical Vendor Oversight Specialist manages third-party vendor relationships throughout the clinical trial lifecycle to ensure study deliverables meet quality and timeline standards. They lead vendor performance monitoring, risk mitigation, and cross-functional collaboration to ensure compliance with regulatory requirements and internal policies.
The FSP Functional Lead provides global strategic direction and oversight for the Medical Writing portfolio, ensuring performance excellence through effective team management. This role also drives business growth by building client relationships, managing budgets, and implementing process improvements across the organization.
The Technical Sales Specialist will drive sales of GeneArt gene synthesis and cloning services by consulting with researchers to provide comprehensive molecular biology workflow solutions. This role involves building strong scientific relationships, executing territory business plans, and collaborating with cross-functional teams to expand market penetration.
Provide technical support, training, and application expertise for LC-MS and HPLC platforms to ensure customer success. Collaborate with sales, marketing, and R&D teams to develop new applications and drive business growth through technical excellence.
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 Medical Director will lead medical safety evaluation and risk management efforts, including the review of adverse events and clinical outcomes. They will also provide medical consultation to the team, manage signal detection activities, and ensure compliance with regulatory guidelines.
The Central Review Manager performs centralized review and approval of clinical monitoring visit reports to ensure consistency and protocol compliance. They also liaise with clinical monitoring staff and evaluate site performance, subject safety, and study processes based on monitoring data.
The Sales Representative is responsible for managing sales of research products and services within a defined territory to ensure market penetration and profitability. They will develop customer relationships, conduct sales calls, and maintain accurate records while collaborating with cross-functional teams.
The Senior Technical Sales Specialist will manage and grow the sales funnel for single-use technologies within the BioProduction Group. They will collaborate with account managers and field application scientists to develop growth strategies and drive new product adoption.
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, data verification, and maintain collaborative relationships with investigative sites to ensure data reliability and subject safety.
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.
The Senior Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol and regulatory compliance. They will also provide mentorship to junior team members and collaborate with cross-functional teams to resolve study issues.
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.
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 specialist will document, analyze, and improve business processes to support operational excellence and audit readiness. They will partner with cross-functional stakeholders to translate requirements into structured process models and support continuous improvement initiatives.
The Inside Sales Representative will grow sales of research products and services by developing and maintaining effective customer relationships. They will implement sales strategies, manage pricing, and conduct market research while working independently and across functional teams.
The role involves identifying and qualifying new business opportunities within the biotech sector while managing a portfolio of accounts. You will collaborate with internal teams to prepare proposals and serve as the primary commercial contact for clients.
Drive sales growth in the clinical trials division by identifying new target clients and molecules while managing existing account relationships. Develop and implement strategic sales plans to expand market share for clinical packaging, labeling, and distribution services.
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.
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 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.
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.
The Account Manager III will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. They will provide tailored scientific solutions to customers through a combination of virtual engagement and in-person visits.
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 Clinical Research Associate II monitors investigator sites to ensure protocol compliance, data accuracy, and adherence to ICH-GCP guidelines. They manage site processes, conduct risk-based monitoring, and facilitate communication between investigative sites and project teams.
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 Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They will perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Senior 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 site documentation, and facilitate communication between investigative sites and the project team.
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 Field Service Engineer 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 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.
The specialist will perform and oversee daily pharmacovigilance activities, including the collection, monitoring, and assessment of safety information. They will also collaborate with project teams, manage clinical study administration, and mentor less experienced staff.
The Senior Manager will develop and implement business strategies to expand market presence and drive growth within the qPCR sector. They will manage key account relationships, identify new business opportunities, and coordinate with cross-functional teams to execute sales initiatives.
The Field Service Engineer will install, maintain, troubleshoot, and repair analytical instrumentation including chromatography and trace elemental systems. They will also manage service schedules, complete documentation, and build trusted relationships with customers to maximize laboratory productivity.
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.
You will provide expert contract review, drafting, and negotiation support for commercial agreements within the legal function. Additionally, you will manage the contract lifecycle while ensuring compliance with corporate policies and regulatory requirements.
The specialist will facilitate site start-up activities, including essential document collection and review to ensure study timelines are met. They will also partner with internal teams and CROs to resolve activation delays and maintain accurate eTMF records.
The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, consistency, and optimal performance throughout the project lifecycle. They also serve as the primary point of contact for clinical project teams and monitor project financial status and operational risks.
The Senior Clinical Trial Manager oversees the technical and operational aspects of clinical trials, ensuring deliverables meet quality, time, and budget expectations. They coordinate start-up activities, manage clinical teams, and serve as the primary point of contact for study sponsors.
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.
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 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.
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 Technical Sales Specialist will drive revenue growth and customer success by providing technical expertise for the Proteomic Workflows & Beads portfolio. They will collaborate with cross-functional teams to implement sales strategies and maintain strong relationships with key accounts.
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 Senior Product Specialist is responsible for driving revenue growth by selling diagnostic capital equipment and consumables to healthcare partners. They will prospect for new business, support sales representatives with technical expertise, and implement strategic sales plans within their assigned territory.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Project Manager is responsible for leading all aspects of client projects, from initial discussions and requirement development to final completion. They must maintain continuous communication with internal departments and external customers while ensuring high-quality work and financial accuracy.
Provide advanced remote technical support for analytical instrumentation including Ion Chromatography and Liquid Chromatography systems. Collaborate with cross-functional teams and customers to troubleshoot complex hardware and software issues while ensuring an exceptional customer experience.
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 Senior Safety Reporting Coordinator manages the submission, tracking, and archiving of safety reports while providing administrative support to the Pharmacovigilance department. They also lead projects, mentor team members, and ensure compliance with standard operating procedures.
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.
Drive sales revenue for downstream workflow products by identifying new business opportunities and managing existing biopharma accounts. Collaborate with internal teams to provide technical solutions and ensure accurate sales forecasting for the assigned territory.
Develop and execute comprehensive channel strategies to expand market presence across pharmaceuticals, biotechnology, and industrial segments. Build and maintain strong relationships with distribution partners while optimizing the channel network to drive business growth.
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 CRM systems.
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.
The role involves monitoring investigator sites using a risk-based approach to ensure data accuracy and regulatory compliance. Responsibilities include conducting site initiations, close-outs, and mentoring new team members while maintaining communication between sites and clients.
The CRA Level II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance using a risk-based approach. They manage site documentation, conduct remote and on-site visits, and maintain collaborative relationships with investigative sites to guarantee data reliability.
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.
Achieve territory revenue goals by pursuing sales opportunities and developing a robust pipeline with current and potential customers. Collaborate with channel partners and promote the broad product portfolio to maximize company results.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring in accordance with SOPs. Assist CRAs with site management tasks, document collection, and the reconciliation of study data and payments.
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.
The role involves independently directing systematic literature review (SLR) projects, from defining research questions and designing search algorithms to synthesizing evidence. Additionally, the position requires managing project timelines, budgets, and leading client communications while overseeing junior staff.
Lead a field sales team to drive revenue growth and market expansion through strategic initiatives and customer relationships. Collaborate across divisions to deliver scientific solutions and achieve growth targets.
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.
Manages day-to-day operations, resource allocation, and project timelines for the Clinical Data Management programming team. Provides technical leadership in database design and testing while overseeing staff performance and professional development.
Performs clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data reliability and maintain audit readiness.
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 representative is responsible for selling research products and services within a defined territory while maintaining effective customer relations. Key duties include performing sales calls, researching competitor activity, and managing pricing to ensure profitability.
Lead engagement with strategic semiconductor customers to drive revenue and growth for a portfolio exceeding $100M in annual business. Manage a team of strategic account managers and build executive-level relationships to facilitate the adoption of Thermo Fisher solutions.
The Global Study Lead is responsible for the end-to-end operational strategy, planning, and execution of global clinical studies. This includes leading cross-functional teams, managing vendors and budgets, and ensuring regulatory compliance across multiple regions.
The Project Manager serves as the primary lead and sponsor contact, accountable for the overall delivery of cross-functional projects regarding quality, time, and cost. They are responsible for managing customer expectations, financial stewardship, and ensuring compliance with regulatory and organizational policies.
The role provides administrative and financial support for processing payments to investigative sites while ensuring adherence to contracts and country regulations. Key duties include data compilation, managing site relationships, and training study teams on payment processes.
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.
The role involves monitoring investigator sites using a risk-based approach to ensure protocol compliance and data reliability. Responsibilities include conducting site visits, managing essential documentation, and maintaining collaborative relationships with investigative sites.
Manages the full life cycle of basic translation project process flows, specifically focusing on linguistic validation. Coordinates the work of linguists and desktop publishers while maintaining client relationships and tracking project KPIs.
Manages the full life cycle of basic translation project process flows, specifically focusing on Linguistic Validation workflows. Coordinates the work of linguists and specialists while maintaining client relationships and tracking project KPIs.
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.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation and data reliability. They conduct remote and on-site visits, perform root cause analysis for site failures, and maintain collaborative relationships with investigational sites.
Design and develop scalable digital applications and prototypes to improve operational efficiency and enable AI capabilities. Collaborate with stakeholders to translate business challenges into technical solutions and high-fidelity wireframes.
Manage and oversee contractual aspects of clinical trials, including drafting and negotiating high-value agreements like CTAs and CDAs. Ensure compliance with international regulations and provide guidance to project teams and junior specialists.
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 Site Contract Specialist is responsible for drafting, negotiating, and finalizing agreements with study sites while ensuring compliance with budgetary and legal parameters. They coordinate with internal teams to align contractual activities with site activation timelines and manage operational risks.
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.
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.
Draft, review, and negotiate agreements with study sites while ensuring compliance with budgetary and contractual parameters. Coordinate with internal functional teams to align site startup activities and achieve target cycle times for site activation.
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 Lead Biostatistician serves as the statistical lead for high-profile pharmacovigilance and safety-focused projects, designing studies and developing statistical analysis plans. They provide strategic leadership for real-world evidence generation and mentor junior biostatisticians to ensure quality and accuracy.
Responsible for the on-site installation, alignment, and calibration of sophisticated electron microscopy systems at customer sites. This includes diagnosing technical issues, providing repair support, and training users on system operation and maintenance.
Manage the preparation, review, and coordination of country-specific regulatory submissions in alignment with global strategies. Serve as the primary contact for regulatory authorities and internal clients to ensure timely site activation and compliance.
Drive sales growth and customer success for advanced analytical and scientific instruments. Develop and expand customer relationships across diverse markets by representing a portfolio of instruments, consumables, and services.
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.
Accelerate commercial growth across the APJ region through direct customer engagement and strategic distributor partner management. Lead business development initiatives to expand presence in Quality Control, Therapeutic Drug Monitoring, and Toxicology markets.
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.
Lead patient-centric medical writing programs focusing on Informed Consent Forms (ICFs) and manage complex projects. Collaborate with cross-functional teams and clients to ensure the quality and flawless delivery of research documents.
The CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing required documentation. They conduct remote and on-site visits to guarantee subject rights, data reliability, and audit readiness.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation and data reliability. This includes conducting remote and on-site visits, performing root cause analysis for site failures, and maintaining collaborative relationships with investigative sites.
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.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage the full sales cycle from RFP strategy and proposal development to contract negotiation and client satisfaction.
Manages the full life cycle of basic translation projects, including assigning work to linguists and desktop publishers. Responsible for tracking project progress, managing client relationships, and ensuring financial and administrative completion.
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.
Lead the collection, organization, and analysis of qualitative data to build a best-in-class research center of excellence. Manage staff, vendors, and AI-enabled technologies while developing business plans and quality assurance processes.
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.
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.
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.
Manage and grow a portfolio of high-level customers in academia, pharma, and biotech across Western Canada to increase revenue for Olink products. Develop strategic sales plans and serve as a trusted advisor to help customers address research questions in real-time biology and drug development.
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.
Maintain regulatory compliance and drive continuous improvement of quality systems across commercial sites in Europe. Responsibilities include managing nonconformities, conducting audits, overseeing supplier quality, and maintaining the data infrastructure for the IES EMEA Quality Team.
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.
Execute regional marketing plans for the Protein Diagnostics portfolio across APMEA to accelerate customer adoption and commercial growth. Partner with global and local stakeholders to adapt campaigns and drive demand generation within healthcare systems.
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.
Perform centralized review and approval of clinical monitoring visit reports to ensure consistency and compliance across projects. Act as a liaison between the review team and project leads while providing training and mentoring to junior managers.
The role involves monitoring investigator sites using a risk-based approach to ensure data accuracy and regulatory compliance. Responsibilities include conducting site visits, managing essential documents, and facilitating communication between sites and the client company.
The role involves monitoring investigator sites using a risk-based approach to ensure data accuracy and compliance with protocols and regulatory obligations. Responsibilities include conducting site visits, managing essential documents, and facilitating communication between sites and the client company.
The Sales Representative is responsible for selling research products and services within a defined territory while maintaining effective customer relations. Key duties include performing sales calls, researching competitor activity, and managing pricing to ensure profitability.
Lead the coordination and oversight of medical projects, ensuring high-quality delivery and successful execution throughout the study lifecycle. Responsibilities include reviewing safety data, managing project financials, and leading cross-functional teams and process improvements.
Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Manage project implementation, forecasting, and communication with stakeholders and investigator sites.
Perform and coordinate all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conduct remote and on-site visits to assess data reliability and maintain audit readiness for pharmaceutical trials.
Define and govern the Ophthalmology portfolio strategy to drive growth and service differentiation. Lead high-value executive client engagements and set medical/scientific quality standards across global proposals and trial support.
Manage the performance and workload of Medical Writers while overseeing the preparation and quality of regulatory deliverables. Coordinate resource planning, develop training programs, and interact with business development to prepare project proposals and budgets.
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.
The Account Manager will develop and implement strategic sales plans to increase revenue and build lasting customer relationships. They will serve as a trusted advisor, providing tailored scientific solutions through consultative selling and cross-functional collaboration.
The role involves monitoring investigator sites using a risk-based approach to ensure protocol and regulatory compliance. Responsibilities include conducting site visits, managing essential documentation, and maintaining collaborative relationships with investigative sites.
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 Senior CRA is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting on-site and remote visits, managing essential documentation, and maintaining relationships with investigative sites.
The role focuses on converting contract renewal quotations into purchase orders for existing customers through direct interaction via email and telephone. The specialist is responsible for achieving sales targets, upselling services, and collaborating with Customer Care Centers to ensure alignment on renewals.
The Clinical Trial Manager is responsible for achieving final clinical deliverables and ensuring 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.
Provide internal legal support for West Europe with a focus on France, including drafting and negotiating various commercial agreements. Act as a strategic partner to leadership to implement legal processes and ensure compliance with healthcare and anti-gift laws.
Coordinate and prepare local regulatory and ethical submissions in alignment with global strategies for clinical trials. Manage site start-up activities and maintain accurate trial status information in tracking databases.
Coordinate and facilitate project activities for clinical trials, serving as a cross-functional liaison and providing administrative and technical support. Manage study-specific documentation, perform file reviews, and support the onboarding and training of new staff.
The Senior Medical Writer is responsible for developing high-quality clinical and regulatory documents such as study reports and protocols. They will collaborate with cross-functional teams and mentor junior writers to ensure compliance with regulatory standards.
Manage and oversee contractual aspects of clinical trials, including drafting and negotiating high-value agreements like CTAs and CDAs. Ensure all contracts comply with local and international regulations while collaborating with internal legal and clinical teams.
The CRA II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance through on-site and remote visits. They manage site documentation, conduct root cause analysis for process failures, and maintain collaborative relationships with investigative sites.
The role is responsible for measuring, optimizing, and forecasting the performance of multi-channel patient recruitment campaigns for clinical trials. It involves translating recruitment data into actionable insights to accelerate enrollment and reduce site burden.
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 Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation. They conduct remote and on-site visits, perform data verification, and maintain collaborative relationships with investigative sites.
Coordinate and prepare local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. Act as the key country-level contact for regulatory activities and maintain accurate trial status tracking in databases.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation. They perform risk-based monitoring, conduct site visits, and maintain collaborative relationships with investigative sites to guarantee data reliability.
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.
Identify and develop new business opportunities while nurturing customer relationships to drive market growth. Provide innovative scientific product solutions and collaborate with cross-functional teams to advance research and healthcare outcomes.
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.
Provide onsite repairs, preventive maintenance, and installation of IDD analyzers within hospitals and commercial laboratories. Collaborate with internal partners and provide technical training to biomedical engineering technicians.
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.
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.
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.
Drive testing initiatives for generative AI and clinical trial technology using advanced manual testing practices. Design and execute test cases, perform API and integration testing, and validate data using SQL queries.
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.
Coordinate site activation and regulatory submissions to ensure clinical trials are initiated efficiently and in compliance with local regulations. Partner with cross-functional teams to manage submission strategies, site documentation, and start-up timelines.
Coordinate and prepare local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. Act as the primary country-level contact for regulatory activities and maintain accurate trial status tracking in databases.
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 Medical Writer authors routine and complex clinical regulatory documents, including study reports, protocols, and INDs. They collaborate with cross-functional teams to ensure document accuracy and mentor junior medical writers to maintain high-quality deliverables.
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 site documentation, and coordinating with clinical team managers.
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.
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.
The Lead Data Engineer is responsible for designing, building, and maintaining scalable data pipelines and platforms to support business operations. This includes optimizing data models, ensuring data governance, and collaborating with analytics teams to meet data requirements.
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.
Drive revenue growth and customer success by providing technical leadership and consultative sales solutions for BioProduction cell culture portfolios. Act as a trusted advisor to customers, conducting product demonstrations and managing complex sales cycles to support scientific advances.
Lead and develop commercial teams to drive strategic growth and achieve revenue targets across the biosciences portfolio. Implement effective sales strategies and manage customer relationships to expand market share globally.
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.
The Field Service Engineer will install, maintain, and troubleshoot chromatography devices while ensuring compliance with regulatory requirements. They will also collaborate with customer care teams to schedule service visits and maintain strong customer relationships.
Provide advanced scientific and technical expertise to customers and internal teams regarding LC-MS and HPLC solutions for Pharma and Biopharma applications. Deliver product training, support method development, and act as a trusted scientific advisor for complex analytical challenges.
Manage a portfolio of complex projects for strategic accounts, overseeing technical implementations and process improvements. Coordinate with cross-functional teams and stakeholders to ensure successful project delivery and client satisfaction.
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.
Ensure compliance with global regulations by interpreting guidelines and developing regulatory strategies for innovative products. Support the entire product lifecycle and improve regulatory information systems to enable business growth and patient safety.
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.
Perform and coordinate all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conduct remote and on-site visits to assess data reliability and maintain audit readiness for oncology trials.
Lead complex safety projects and manage CEC/DSMB activities, including charter development and electronic adjudication system builds. Act as a liaison between the company and sponsors to ensure successful pharmacovigilance implementation and regulatory compliance.
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.
The QC Coordinator manages the assignment and tracking of quality check requests for translation projects with internal and external linguists. They are responsible for maintaining delivery schedules, managing client communications, and recording KPI data for business analysis.
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.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage the full sales cycle from RFP strategy and proposal development to contract negotiation and client satisfaction.
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.
The role involves coordinating clinical monitoring and site management, including source data verification and ensuring protocol and regulatory compliance. It requires conducting on-site and remote visits while collaborating with cross-functional teams to maintain audit readiness.
Manage the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. Serve as the primary contact for regulatory authorities and internal clients to ensure timely site activations and compliance.
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, while providing consultation to clients and investigators.
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.
Manages the preparation and coordination of country-specific regulatory submissions in alignment with global strategies. Serves as the primary contact for investigators and regulatory authorities to ensure timely site activation and compliance.
Coordinates and facilitates clinical trial activities, providing administrative and technical support to the project team. Manages study documentation, performs file reviews, and acts as a liaison for cross-functional project initiatives.
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.
The Project Manager serves as the primary contact for sponsors and is accountable for the overall delivery of cross-functional projects regarding quality, time, and cost. They are responsible for managing customer expectations, financial stewardship, and ensuring compliance with organizational and regulatory policies.
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.
Provide medical leadership and support for clinical trials in nephrology, including protocol creation and real-time medical monitoring. Act as the primary medical liaison between the sponsor and internal departments to ensure subject safety and study compliance.
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 Clinical Data Team Lead manages end-to-end external data acquisition activities, including vendor integrations and data ingestion for clinical studies. They act as a liaison between departments and clients while ensuring all data management deliverables are audit-ready and compliant with regulatory standards.
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 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.
The Senior 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 site-related documentation.
The Clinical Trial Manager is responsible for achieving final clinical deliverables within specified timelines and budgets while ensuring compliance with ICH GCP standards. They manage clinical operational aspects, lead team meetings, and collaborate with cross-functional departments to maintain project quality and resource allocation.
The Medical Director provides medical oversight for clinical trials, ensuring adherence to regulatory requirements and good clinical practice. They also manage safety data, perform signal detection, and provide medical consultation to project teams and clients.
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 Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They manage study documentation, perform file reviews, and act as a liaison across functional departments to maintain high quality standards.
Perform and oversee day-to-day pharmacovigilance activities, including the collection, monitoring, and assessment of safety information. Collaborate with project teams, investigators, and clients to ensure operational excellence and regulatory compliance.
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-specific issues through risk-based monitoring.
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 Safety Scientist is responsible for planning, coordinating, and delivering signal detection and product safety activities across various levels of complexity. They also support the mentoring of junior colleagues, contribute to process development, and lead small functional service provider projects.
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.
As a Site Contract Specialist, you will prepare and negotiate contracts, as well as finalize the contract process. You will draft, review, negotiate, and finalize agreements with study sites in accordance with local processes.
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 role involves developing and implementing comprehensive business development strategies, analyzing market trends, and positioning solutions to meet customer needs across pharmaceutical, biotech, and research organizations. Responsibilities include managing the full sales cycle from lead generation through contract negotiation while maintaining detailed CRM records.
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.
The Account Manager is responsible for selling and supporting all Chromatography and Mass Spectrometry Division products, maintaining customer relationships, and driving strategic growth within assigned accounts. This role serves as the primary point of contact, providing sales expertise and leading all commercial activities across the CMD portfolio.
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.
The Clinical Research Associate 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 involve monitoring investigator sites using a risk-based approach, identifying failures, implementing corrective actions, and ensuring data reliability.
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.
As a Clinical Data Associate II, you will lead advanced data review and cleaning activities to ensure data integrity and inspection readiness. You will manage complex queries, perform data reconciliations, and produce status reports for stakeholders.
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.
