The Clinical Trial Coordinator provides administrative and technical support for clinical trials, including site activation, file reviews, and regulatory document management. They ensure trial activities are performed on time and within budget while maintaining compliance with SOPs and regulatory guidelines.
The Commercial Finance Analyst leads cross-functional processes to ensure clinical trial contract proposals and budget modifications are completed accurately. They manage the proposal bid process, determine resource allocations, and maintain positive client relationships throughout the negotiation lifecycle.
The Senior Upstream Process Engineer will lead front-end engineering and proposal development for capital bioprocessing projects, including cell culture media and bioreactor systems. This role serves as a technical leader, engaging with customers to translate process requirements into robust, commercially viable solutions.
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.
Perform on-site installation, maintenance, and repair of sophisticated electron microscopy equipment. Provide technical training to customers and support field service operations while maintaining positive client relationships.
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 Associate Trade Compliance Manager will develop and implement import/export strategies for clinical studies while ensuring full compliance with local and global regulations. They will serve as the primary point of contact for trade compliance matters and coordinate with stakeholders to prevent operational obstacles.
The Senior 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.
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 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 sponsors while managing essential documentation and trial close-out procedures.
Lead computerized system validation activities for regulated applications throughout the system development lifecycle. Partner with cross-functional teams to ensure software solutions meet business needs, regulatory requirements, and data integrity standards.
The Global Cold Chain & HVAC Leader provides technical leadership and functional expertise to establish global engineering standards for temperature-controlled storage and HVAC systems. This role drives network capability, manages capital planning, and ensures compliance and business continuity across the CTD network.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including site preparedness, remote monitoring, and document collection. They also assist with system updates, vendor coordination, and reconciliation tasks to ensure compliance with SOPs and regulatory guidelines.
The Data Reviewer ensures the integrity and quality of laboratory and chromatographic data by verifying compliance with analytical methods and GMP/GLP standards. They communicate findings to laboratory staff and support process improvement initiatives to maintain high documentation standards.
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 Start-up Team Manager oversees complex site operations, ensuring regulatory compliance and effective site activation for clinical studies. They manage financial and contractual aspects while facilitating collaboration between internal teams and trial sites to meet project timelines.
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.
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 associate will research and qualify business opportunities with biotech companies while managing early-stage client accounts. They will collaborate with internal teams to prepare proposals and serve as the primary commercial point of contact for a portfolio of accounts.
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.
Provide advanced technical expertise and leadership for high-performance electron microscopy and analytical systems. Act as a technical liaison between field service, R&D, operations, and customers to ensure optimal system performance.
The Clinical Trial Coordinator II provides administrative and technical support for clinical trials, including site activation, file reviews, and regulatory document management. They ensure trial activities are performed on time and within budget while maintaining compliance with SOPs and regulatory guidelines.
The 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 Senior Biostatistician will serve as the statistical lead on high-profile client-facing projects and collaborate with cross-functional teams. They are responsible for designing studies, developing statistical analysis plans, and providing strategic leadership for real-world evidence generation.
The role involves providing strategic and operational regulatory leadership for late-stage global development programs across the EU, UK, and Switzerland. Responsibilities include managing Marketing Authorisation Applications, coordinating cross-functional submissions, and ensuring compliance with European regulatory requirements.
The Country Approval Specialist manages and coordinates local regulatory submissions and site start-up activities in alignment with global submission strategies. They provide regulatory advice to internal clients and ensure all trial status information is accurately maintained in tracking databases.
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.
Design and develop sophisticated software solutions using Salesforce technologies to support global life sciences operations. Collaborate with cross-functional teams in an agile environment to architect, implement, and optimize robust applications.
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 Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also manage study documentation, perform file reviews, and act as a liaison for cross-functional project initiatives.
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 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 oversee site-level activities to ensure compliance with regulatory standards.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, 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.
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 Program Manager will lead strategic sourcing initiatives and cross-functional programs to enhance comparator services and drive business growth. They will also act as a product champion, leveraging AI and analytics to optimize sourcing strategies while serving as a strategic advisor to Biopharma customers.
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.
Perform day-to-day adverse event reporting and pharmacovigilance activities within a highly regulated environment. Coordinate project implementation, maintain regulatory safety reports, and provide guidance to team members.
The Manager, Quality serves as the enterprise validation subject matter expert, responsible for implementing validation strategy, governance, and capability development across the organization. This role acts as the Business Process Owner for validation platforms and partners with cross-functional stakeholders to ensure consistent, risk-based validation practices.
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 Principal Programmer Analyst oversees statistical and bioinformatics programming for clinical trials, ensuring operational excellence from design through reporting. They also provide leadership to project teams, manage client interactions, and contribute to process improvements and department initiatives.
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 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 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 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.
The Biostatistician II leads project teams, manages timelines, and ensures compliance with departmental SOPs for statistical analysis and programming. They also coordinate with data management personnel, provide statistical guidance, and develop statistical analysis plans for clinical research projects.
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 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 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 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.
Define and lead the end-to-end cloud architecture to ensure secure, scalable, and compliant data services. Collaborate with cross-functional teams to implement event-driven, serverless, and containerized solutions while mentoring engineering staff.
You will develop and manage 24-month demand plans while facilitating Sales & Operations Planning (S&OP) processes. Additionally, you will collaborate with cross-functional teams to optimize inventory levels and enhance forecast accuracy.
The Manager of Clinical Operations oversees, trains, and mentors a team while ensuring adherence to company SOPs and regulatory standards. They are responsible for managing project metrics, KPIs, and collaborating with leadership on strategic planning and resourcing.
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.
Generate sales growth through virtual and digital channels while building strong relationships with customers across various scientific markets. Develop and execute strategic sales plans while managing customer relationships through the CRM system.
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 Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. They ensure compliance with SOPs and regulatory guidelines while assisting with site preparedness, document collection, and data reconciliation.
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 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 external clients and collaborate with internal departments to facilitate site startup activities.
The Clinical Research Associate coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They perform on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-level issues.
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 Senior Director leads the commercial strategy and investment engagement lifecycle for biopharma manufacturing expansion projects. They serve as the primary commercial interface for executive stakeholders to drive complex, long-cycle CAPEX sales opportunities.
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 Compliance Specialist is responsible for managing quality compliance activities including document review, approval, and filing. They will also lead process improvement initiatives while collaborating with teams to ensure adherence to quality regulations.
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.
The Principal Country Approval Specialist manages local regulatory submissions and provides strategic regulatory advice to internal clients. They coordinate site start-up activities and serve as the primary contact for investigators and regulatory authorities to ensure timely project execution.
The Sr Principal Scientist will design and implement nonclinical safety strategies for drug candidates from lead optimization through marketing submission. They will also oversee outsourced studies at CROs and collaborate with multidisciplinary teams to ensure regulatory compliance and project success.
The Manager of Clinical Operations oversees, coaches, and manages a team of clinical staff to ensure project deliverables and performance metrics are met. They are responsible for resource allocation, training, and maintaining adherence to regulatory standards and company SOPs.
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 Compliance Specialist II manages day-to-day import/export activities, including classification, screening, and licensing to ensure regulatory compliance. They also collaborate across functions to implement trade policies, conduct audits, and drive process improvements.
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 Account Manager is responsible for selling and supporting chromatography and mass spectrometry products while maintaining long-term customer relationships. They will identify new business opportunities, negotiate contracts, and lead sales strategies to meet quarterly objectives within their assigned territory.
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 Sales Operations Specialist manages operational processes and Salesforce data to support the sales team's execution. They coordinate client meetings, handle RFPs/RFIs, and collaborate with Legal to oversee contractual agreements.
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.
You will generate sales growth through virtual and digital channels while building strong relationships with customers across various scientific markets. Additionally, you will develop strategic sales plans and manage customer relationships using the CRM system to achieve business targets.
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 Contract Coordinator manages Clinical Trial Agreements with research sites and principal investigators globally. They facilitate critical documentation and ensure compliance while supporting the execution of international clinical trials.
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 Assistant CRA 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 reconciliation of study data in accordance with regulatory guidelines.
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.
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 reviewing trial files, maintaining study metrics, and coordinating activities to meet project deadlines.
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 Supplier Marketing Specialist coordinates supplier-funded marketing campaigns from planning through execution, reporting, and invoicing. They act as an operational point of contact for suppliers while maintaining marketing platforms and ensuring financial accuracy.
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 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 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.
Lead a global Language Management team to ensure high-quality, compliant, and scalable language solutions for clinical and life sciences programs. Manage team performance, drive operational excellence, and act as a strategic liaison between Language Services and senior business leadership.
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 II provides administrative, financial, and contractual support for processing payments to investigative sites. They are responsible for calculating billing data, managing investigator fee trackers, and resolving payment-related risks in collaboration with internal and external stakeholders.
The Compliance Specialist manages quality and compliance processes, including conducting internal and external audits and investigations. They also facilitate the tracking of quality activities, maintain client product files, and act as a primary contact for GMP quality and customer technical agreements.
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 DeltaV SQA Engineer will develop and implement comprehensive software test plans and protocols for bioprocessing systems. They will collaborate with cross-functional teams to ensure software quality, compliance with regulatory standards, and the successful execution of verification activities.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, perform file reviews, and maintain study metrics in compliance with SOPs and regulatory 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, conduct site visits, and manage documentation to maintain audit readiness.
Lead a team of service sales representatives to meet financial targets and drive contract revenue growth within the assigned region. Collaborate with cross-functional teams including operations, marketing, and product management to implement strategic account plans and improve internal processes.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol and regulatory compliance. They are responsible for maintaining data reliability, ensuring audit readiness, and fostering collaborative relationships with investigational sites.
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.
The Global Reliability & Maintenance Leader establishes global strategy, standards, and governance for asset reliability and maintenance across the CTD network. This role leads the deployment of maintenance excellence roadmaps and partners with regional leadership to optimize asset performance and reduce operational risk.
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.
The role involves managing the sales process for advanced analytical instruments to state and local government agencies, including law enforcement and public safety markets. Responsibilities include conducting product demonstrations, developing strategic sales plans, and maintaining strong customer relationships to meet bookings targets.
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 Associate Director will lead the development of patient-centric recruitment and engagement strategies to optimize clinical trial performance. They will serve as a subject matter expert, translating client needs into innovative digital solutions and driving growth through persuasive client engagements.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage essential documentation, and facilitate communication between investigative sites and the project team.
The Country Approval Specialist manages and coordinates local regulatory submissions and site start-up activities in alignment with global strategies. They provide regulatory advice to internal clients and ensure all trial status information is accurately maintained in tracking databases.
You will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Additionally, you will provide tailored scientific solutions to customers through a mix of virtual engagement and site visits.
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 Field Service Engineer will install, maintain, troubleshoot, and repair sophisticated analytical and scientific instruments in various laboratory settings. They are responsible for providing exceptional customer service and ensuring all work adheres to GMP and safety standards.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Conducts risk-based monitoring, manages site documentation, and facilitates communication between investigative sites and the project team.
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 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 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.
The Site Payments Associate II provides administrative, financial, and contractual support for processing payments to investigative sites. Responsibilities include compiling data, managing site relationships, resolving payment-related issues, and ensuring adherence to regulatory guidelines.
Provide strategic leadership and oversight for the Medical Writing Functional Service Partnership portfolio to ensure operational excellence. Lead and develop high-performing teams while building strong relationships with clients and internal stakeholders across the organization.
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 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 standards.
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 Services Sales Development Representative III is responsible for driving new service revenue growth and expanding service agreement coverage across the EMEA region. They will proactively identify and convert new business opportunities while managing renewals and maintaining a robust sales pipeline.
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 Senior Operational Bidding Specialist leads the development of complex operational budgets and proposals for clinical research opportunities. They collaborate with cross-functional teams to ensure strategic alignment with client requirements and business objectives.
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 Sales Representative II 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.
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.
Lead and execute global CMC regulatory strategies for biological products while ensuring compliance with US and Canadian regulatory requirements. Manage the preparation, review, and submission of regulatory dossiers and oversee post-approval lifecycle management activities.
The Consultant will implement and optimize Digital Science software by gathering business requirements and translating them into technical specifications. They will act as a trusted advisor to customers, ensuring laboratory operations and data management systems are effectively integrated and compliant.
The Business Analyst will bridge business needs with technology solutions by analyzing processes and gathering requirements. They will collaborate with cross-functional teams to implement innovative solutions and ensure successful project delivery within an agile environment.
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 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 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 Senior Project Coordinator provides administrative and technical support to the Global Clinical Supplies team by managing project documentation, regulatory files, and data repositories. They also assist in report preparation, mentor junior staff, and ensure compliance with GCP and organizational SOPs.
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.
You will drive revenue growth by developing strategic customer relationships and promoting a portfolio of scientific products. Additionally, you will implement sales strategies and identify new business opportunities within your assigned territory.
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 Sales Operations Specialist manages operational processes and Salesforce data to support the sales team in clinical development service offerings. They coordinate client meetings, handle RFPs and RFIs, and partner with Legal to oversee contractual agreements.
The Category Manager will oversee end-to-end product lifecycle management, from strategy development through commercialization and optimization. They will manage key supplier relationships, drive category performance, and collaborate with cross-functional teams to deliver innovative solutions.
The Executive Medical Director provides strategic leadership for pharmacovigilance and medical monitoring across the clinical research lifecycle. This role involves mentoring global teams, ensuring regulatory compliance, and collaborating with cross-functional partners to drive safety and business objectives.
Develop and manage comprehensive demand forecasts while collaborating with cross-functional teams to optimize inventory levels. Facilitate demand review processes, analyze market trends, and provide insights to improve forecast accuracy and support strategic decision-making.
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.
The Clinical Trial Coordinator maintains study documentation, manages investigator files, and oversees clinical study tracking systems to ensure project progress. They also assist with study logistics, coordinate with medical staff, and ensure compliance with regulatory requirements and SOPs.
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.
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 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.
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.
Lead computerized system validation activities for regulated digital and AI applications throughout the software development lifecycle. Partner with cross-functional teams to ensure systems meet business requirements, regulatory standards, and quality expectations.
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 role involves leading and developing high-quality, customer-focused proposals by evaluating RFPs and collaborating with internal teams to define bid strategies. It also requires maintaining accurate bid grids, managing budget assumptions, and presenting bid strategies to senior management.
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, manage documentation, and resolve site-level issues.
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.
Lead strategic projects from initiation through implementation to support global operations strategy within the Life Science Solutions Group. Manage cross-functional teams, project scope, timelines, and stakeholder expectations while ensuring alignment with business goals.
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 Site Contract Specialist manages the end-to-end preparation, negotiation, and finalization of investigator contracts. They collaborate with internal teams and study sites to ensure contractual alignment, risk mitigation, and adherence to project timelines.
The PV Coordinator manages safety documentation, coordinates DSMB/EAC committee meetings, and ensures compliance with regulatory standards. They also facilitate project communications, maintain program files, and perform data entry into tracking systems.
The Strategic Pricing Lead will develop and implement pricing strategies for the DACH region to optimize profitability and market share. This role involves cross-functional collaboration with sales, marketing, and finance to analyze market trends and execute pricing initiatives.
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 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 identifying and mitigating legal, financial, and operational risks.
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.
The Senior Director leads global account strategies to drive enterprise growth and manages a team of Global Account Leaders across multiple regions. They are responsible for building executive-level partnerships and delivering commercial outcomes for flagship pharmaceutical and contract testing laboratory accounts.
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 Field Service Engineer performs installations, repairs, and preventative maintenance on laboratory instruments at customer sites. They also collaborate with internal partners to resolve technical issues and maintain accurate service documentation.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory requirements and internal SOPs.
The Senior Product Specialist drives strategic account growth for autoimmune and IFA testing by implementing testing algorithms and workflow solutions. This role collaborates with sales, marketing, and clinical teams to deliver technical content and accelerate revenue growth across the US market.
The Field Service Engineer II is responsible for performing onsite installations, repairs, and preventative maintenance on laboratory instruments. They also act as a trusted advisor to customers, driving satisfaction and identifying opportunities for service contract sales.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions to ensure timely site activation. They also provide local regulatory strategy advice and serve as a primary contact for investigators and regulatory authorities.
The role involves managing monthly, quarterly, and annual client financial accruals to ensure accurate invoicing and revenue recognition. It also requires serving as a liaison between Operations, Finance, and Procurement to oversee reconciliations and purchase order management.
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 Account Manager will develop and execute strategic sales plans to drive growth for analytical and scientific instruments across various markets. They will build and maintain strong customer relationships while providing consultative solutions tailored to laboratory workflows and business needs.
The Clinical Trial Coordinator provides administrative and technical support for clinical trials, including site activation, documentation maintenance, and vendor management. They ensure study activities are performed accurately, on time, and in compliance with regulatory standards and client requirements.
You will contribute to financial and business objectives by monitoring and analyzing budgets and resource data for a portfolio of clinical research projects. You will also collaborate cross-functionally to oversee financial aspects, manage contract modifications, and identify project risks.
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 Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits, perform root cause analysis, and maintain collaborative relationships with investigative sites.
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 in-person visits.
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 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.
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.
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 Project Manager is responsible for the overall delivery of clinical trials, ensuring quality, timelines, and budget adherence. They lead cross-functional teams and serve as the primary point of contact between the sponsor and the organization.
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 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 corrective actions for site process failures.
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.
The Clinical Trial Manager is responsible for managing all operational and quality aspects of clinical 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 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 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 Account Manager will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. They will provide tailored scientific solutions through consultative selling and collaborate with cross-functional teams to meet sales targets.
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 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 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 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 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 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 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 Product Specialist will drive revenue growth and customer success by providing technical sales expertise for the Olink proteomics platform in the Oncology sector. They will manage the full sales cycle, build relationships with key stakeholders, and collaborate with cross-functional teams to implement effective sales strategies.
The Senior Product Specialist will drive revenue growth for the Specialty Diagnostics portfolio by prospecting new business and managing existing customer accounts. They will provide technical support, deliver presentations, and collaborate with the sales team to meet clinical and operational goals.
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.
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 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 design and develop complex Tableau reports, dashboards, and self-service analytics solutions while administering Tableau Server or Cloud infrastructure. Additionally, you will partner with stakeholders to translate business needs into governed data products and integrate reporting solutions with AWS services.
The Strategic Account Leader is responsible for driving growth and profitability for key Pharma Services Group accounts by developing deep client relationships and strategic account plans. They lead cross-functional teams to manage client portfolios, ensure contract compliance, and deliver harmonized, high-value solutions across global sites.
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.
Provide technical support and training for the Olink proteomics product portfolio while serving as a scientific advisor to customers. Collaborate with sales, marketing, and R&D teams to optimize workflows and drive business growth through technical excellence.
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 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 Medical Scientific Liaison will accelerate the adoption of biomarker assays through peer-to-peer scientific dialogue and expert consultation. They are responsible for identifying key opinion leaders, generating scientific insights, and providing technical expertise to support clinical practice and patient management.
The Project and Budget Coordinator will manage the financial aspects of assigned projects by monitoring budgets, reviewing expenditures, and ensuring resource allocation aligns with project goals. They will collaborate cross-functionally to identify risks, analyze financial data, and provide rationale for budget approvals.
Manage and grow a diverse portfolio of customers across France and Belgium by building long-term partnerships and identifying new sales opportunities. Collaborate with internal teams and product specialists to provide tailored solutions that meet customer scientific and operational needs.
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.
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.
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.
Drive revenue growth for the bioprocess downstream workflow portfolio across France and Belgium by identifying opportunities and building strong customer relationships. Provide technical leadership and consultative support to biopharmaceutical clients to optimize their purification and manufacturing workflows.
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 Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through both remote and on-site visits. They manage site processes, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial lifecycle.
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 Finance Analyst will support commercial finance activities for the LPG and LCD businesses across EMEA, focusing on revenue, pricing, and operational expenditure forecasting. The role involves partnering with commercial leaders to provide forward-looking insights, drive business performance, and support strategic planning initiatives.
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 Senior Medical Director will provide medical monitoring and safety evaluation for clinical trials within the pharmacovigilance department. They are responsible for leading medical aspects of contracted tasks, reviewing safety data, and providing medical consultation to internal teams and clients.
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 essential documentation, and facilitate communication between investigative sites and project teams.
The Senior Director will define and scale the foundational AI platform architecture to support rapid development and deployment of AI-enabled products. This role involves leading cross-functional teams to establish MLOps standards, governance, and reusable AI capabilities across the organization.
The Senior Director defines and enforces AI risk, regulatory compliance, and governance frameworks across the clinical research group. This role partners with engineering and delivery teams to embed governance-by-design into AI systems while ensuring alignment with enterprise and regulatory standards.
The role involves monitoring investigator sites to ensure protocol compliance, data accuracy, and audit readiness through remote or on-site visits. It also requires managing site processes, facilitating communication between stakeholders, and ensuring all clinical trial activities adhere to ICH-GCP guidelines and regulatory standards.
The Senior Director is responsible for building, operating, and scaling end-to-end AI engineering and platform capabilities to drive business impact. This role leads product-aligned engineering teams to deliver production-ready AI solutions while establishing modern AI-native execution layers and automation frameworks.
The Clinical Trial Coordinator provides administrative and technical support to project teams by facilitating project activities and ensuring trial tasks are completed on time and within budget. They also manage study documentation, perform file reviews, and act as a cross-functional liaison to ensure compliance with regulatory standards.
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 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 site performance, manage documentation, and resolve issues in accordance with ICH-GCP guidelines.
The Product Marketing Specialist will conduct market research, competitive analysis, and customer segmentation to support strategic product initiatives. They will also collaborate with cross-functional teams to execute commercialization processes and integrate customer insights into product roadmaps.
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.
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.
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 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.
You will manage key accounts within the pharmaceutical, semiconductor, biotech, and industrial segments to drive revenue growth. This involves developing strategic customer relationships, promoting a portfolio of scientific products, and implementing effective sales strategies.
The Senior CRA manages clinical monitoring and site management activities to ensure trials are conducted according to protocols, ICH-GCP, and regulatory requirements. They perform remote and on-site monitoring, conduct data verification, and maintain effective communication with investigational sites to ensure data quality and patient safety.
Provide bioinformatics helpdesk and application support for NGS and Microarray products by troubleshooting complex workflow and software issues. Manage customer cases end-to-end while collaborating with cross-functional teams to improve product documentation and customer experience.
The Regional Medical Affairs Manager will serve as the scientific leader for precision oncology and molecular diagnostics, fostering collaborations with key opinion leaders and academic institutions. They will drive evidence-generation initiatives and support the implementation of innovative NGS-based diagnostic solutions across the region.
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 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 corrective actions for investigator sites.
The Lead Qualification Representative connects marketing initiatives with sales execution by qualifying leads and routing them to appropriate commercial resources. They also manage customer outreach, track interactions in the CRM, and provide actionable insights to improve marketing effectiveness.
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 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.
The Senior Manager provides strategic and operational leadership to EMEA Technical Sales Specialist teams to ensure growth targets are met across product lines. They are responsible for sales process optimization, funnel management, and driving business development in collaboration with regional stakeholders.
Lead a team of technical sales specialists to drive strategic growth and market share across various scientific sectors. Develop and execute commercial strategies while fostering strong customer relationships and managing sales pipelines.
The Field Service Representative will install, maintain, troubleshoot, and repair complex analytical and scientific instruments across various customer settings. They are also responsible for providing exceptional customer service, training clients on equipment operation, and documenting all service activities.
Develop and edit high-quality clinical and regulatory documents such as study reports, protocols, and submissions. Collaborate with cross-functional teams to ensure document accuracy, regulatory compliance, and adherence to project timelines.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
The 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 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 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.
Develop and execute strategic sales plans to drive growth for analytical reagents and discovery chemicals within the assigned territory. Coordinate with distribution teams and internal colleagues to conduct technical seminars, product launches, and customer-focused sales activities.
The Due Diligence Lead is responsible for evaluating the feasibility, risks, and benefits of significant operational pursuits, including restructuring and large capital expenditures. This role collaborates with executive leadership to develop proposals from initial concept to business approval through rigorous data analysis and financial modeling.
Field Service Engineers manage customer relationships and provide technical support, including installation, repairs, and preventative maintenance of chromatography and mass spectrometry equipment. They are responsible for meeting service level agreements and internal key performance indicators while ensuring high levels of customer satisfaction.
The Field Service Engineer will conduct on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and act as a subject matter expert for system troubleshooting and documentation.
The Site Search Operations Specialist will optimize site search performance by analyzing search data, implementing search rules, and collaborating with cross-functional teams. They will also define requirements for search enhancements and provide training and best practices to business stakeholders.
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 Assistant CRA 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 reconciliation tasks to ensure compliance with regulatory guidelines and SOPs.
The Senior Recruiter will manage full-cycle recruitment for diverse roles while acting as a strategic talent advisor to business partners. They are responsible for developing sourcing strategies, building talent pipelines, and providing data-driven insights to hiring managers.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will perform on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-level issues.
The Supervisor will lead a team of Field Service Engineers, managing their performance, development, and daily scheduling. They will also facilitate team communication, handle customer escalations, and perform field service activities for approximately 50% of their working hours.
You will lead and support a team of field service engineers to ensure high-quality service delivery and operational excellence. The role involves coordinating service activities, managing team performance, and maintaining strong relationships with customers and internal stakeholders.
The Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions and site start-up activities. They also lead complex site contract and budget negotiations while ensuring compliance with global and local regulatory standards.
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 Project Manager leads and coordinates central laboratory activities for clinical trial programs, ensuring project performance and client satisfaction. They act as the primary liaison between sponsors and internal departments while maintaining study documentation and ensuring regulatory compliance.
The Clinical 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 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 Field Service Engineer will perform on-site installation, preventive maintenance, and repairs on electron microscopy systems. They are also responsible for providing technical support to customers and ensuring effective operation of the instrumentation.
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 will install, maintain, troubleshoot, and repair sophisticated analytical and scientific instruments for customers in research and industrial settings. They are responsible for providing exceptional customer service, documenting service activities, and training customers on equipment operation.
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 Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They must provide exceptional customer service while ensuring equipment operates correctly and supporting customers with technical training.
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.
The Country Approval Specialist manages and coordinates country submissions to ensure prompt site start-up and adherence to study timelines. They also collaborate with internal teams and CROs to review essential site documents and resolve escalated issues.
The Field Application Scientist provides scientific and technical expertise to customers, supporting the implementation and use of imaging and detection platforms. They collaborate with sales and product teams to optimize experimental workflows, troubleshoot scientific challenges, and deliver customer training.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global submission strategies. They act as the primary contact for regulatory activities and ensure site start-up processes are aligned with project timelines.
The role involves developing and implementing strategies to drive sales growth within assigned pharmaceutical territories across various drug modalities. You will manage the full sales cycle, build executive-level customer relationships, and collaborate cross-functionally to deliver integrated solutions.
The Country Approval Specialist manages, prepares, and coordinates local regulatory submissions in alignment with global strategies. They also act as a key contact for ethical and regulatory activities while ensuring site start-up processes meet critical timelines.
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 activation timelines are met while managing legal and financial risks.
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 Contract Specialist will negotiate clinical trial agreements, budgets, and payment terms while managing the contract lifecycle for site-related activities. They will collaborate with cross-functional teams to ensure compliance with regulatory requirements and facilitate timely study execution.
The specialist will draft, review, and negotiate site agreements and investigator grant budgets while ensuring compliance with internal and client processes. They will also coordinate with internal functional teams to ensure site startup activities align with contractual timelines and critical paths.
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 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, monitor trial performance, and ensure compliance with ICH GCP and corporate policies throughout the study lifecycle.
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 analyst will support sales incentive compensation for North American field sales teams and manage sales data quality. They will also coordinate territory mapping and provide ad-hoc reporting to support commercial business goals.
Drive revenue growth by identifying and securing new business opportunities in drug product development and commercial manufacturing services. Manage client relationships, lead proposal development, and represent the company at industry conferences and tradeshows.
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 the project team.
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.
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 Principal Clinical Trial Coordinator manages clinical project logistics, including eTMF oversight, site start-up activities, and document quality control. They provide technical and administrative support to study teams to ensure project deliverables meet contract requirements and regulatory standards.
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.
You will contribute to financial and business objectives by monitoring and analyzing budgets and resource data for a project portfolio. You will also collaborate cross-functionally to oversee financial aspects of projects and prepare estimates for contract modifications.
Lead cross-functional project teams to manage product development and on-market improvements for transplant diagnostics. Ensure projects meet regulatory guidelines, quality standards, and business objectives while maintaining clear communication with stakeholders.
The Sr OEM Sales Representative will manage sales, business development, and commercial relationships within an assigned territory for the Laboratory Consumables portfolio. They are responsible for building customer partnerships, leading cross-functional teams, and driving growth through strategic contract management and business reviews.
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 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 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 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.
The Executive Director will lead strategic growth and relationship management for key biopharma and biotech partnerships. They will oversee account teams to deliver exceptional customer experiences while expanding the company's market presence across clinical and pharmaceutical services.
The Quotation Specialist will manage contract proposals, tender submissions, and budget processes while coordinating sales activities from opportunity identification to execution. They will also optimize internal processes and provide actionable data insights to drive business growth and customer satisfaction.
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 Strategic Alliances Manager will lead and cultivate partnerships with pharmaceutical companies to integrate next-generation sequencing technologies into companion diagnostics. Responsibilities include managing contractual agreements, leading steering committee meetings, and addressing issues to ensure the success of each alliance.
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.
Lead large strategic programs and complex portfolios that contribute to global business transformation initiatives. Build and guide high-performing teams while serving as a trusted advisor to senior leadership on portfolio governance and resource optimization.
Draft, review, and negotiate clinical trial site agreements while ensuring compliance with budgetary and contractual parameters. Coordinate with internal teams to align site startup activities with project timelines and manage risk escalation.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. They ensure compliance with SOPs and regulatory guidelines while assisting with site preparedness, document collection, and data reconciliation.
The Account Manager will develop and implement strategic sales plans while managing key account relationships to drive revenue. They will collaborate with cross-functional teams to provide tailored scientific solutions and ensure customer satisfaction.
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 Senior/Principal Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions to ensure timely site activation. They provide regulatory strategy advice, serve as a primary contact for investigators and authorities, and oversee project-related documentation.
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.
Develop and implement strategic plans to grow the Allergy & Autoimmunity portfolio and build lasting relationships with medical laboratories and hospitals. Drive 'Patient Pathway' initiatives and manage commercial forecasting and reporting via Salesforce.
Conduct remote and on-site monitoring visits to ensure clinical trials comply with protocols, ICH-GCP guidelines, and regulatory requirements. Manage site documentation, perform data verification, and maintain collaborative relationships with investigational sites.
The CRA Level II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance through on-site and remote visits. They manage site documentation, conduct data verification, and maintain collaborative relationships with investigative sites to guarantee subject safety and data reliability.
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.
The Business Development Manager is responsible for driving growth by identifying and commercializing integrated laboratory workflow solutions across Thermo Fisher's portfolio in Australia and New Zealand. The role involves partnering with customers to optimize laboratory operations and coordinating cross-divisional teams to deliver seamless, value-based solutions.
Provides administrative and technical support for clinical trials, focusing on site activation and audit readiness. Responsibilities include managing eTMF systems, reviewing investigator files, and coordinating regulatory documentation.
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 management and remote monitoring activities. Assist CRAs with site preparedness, document collection, and the reconciliation of study data in accordance with SOPs.
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.
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.
Support field sales activities and customer engagement across Germany, the Netherlands, and V4 countries for downstream bioproduction portfolios. Collaborate with account managers to position technical solutions for chromatography, buffer outsourcing, and production chemicals.
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
The role involves managing and mentoring Clinical Team Managers to ensure the successful execution of clinical deliverables within assigned projects. It also requires overseeing budgeting, resource allocation, and the implementation of performance metrics for the clinical management group.
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.
Manage trial patient payments and oversee site payment processes. Ensure financial accuracy and compliance within the FSP framework.
The Field Service Engineer is responsible for the installation, maintenance, repair, and qualification of analytical and scientific instruments. They provide technical support to customers, manage service documentation, and promote service offerings during site visits.
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.
The CRA I coordinates clinical monitoring and site management to ensure protocol and regulatory compliance. They conduct site visits, manage documentation, and maintain collaborative relationships with investigational sites to guarantee data reliability.
Manages the full life cycle of translation projects, including assigning work to linguists and desktop publishers. Responsible for tracking project progress, managing client relationships, and ensuring financial and administrative completion.
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 Account Manager III is responsible for increasing revenue and building lasting customer relationships by representing a portfolio of scientific products and services. The role involves developing strategic sales plans and providing tailored solutions through consultative selling to help customers achieve scientific goals.
Install, maintain, calibrate, and repair laboratory equipment such as incubators, centrifuges, and freezers to maximize uptime. Manage daily service operations including scheduling, reporting, and collaborating with cross-functional teams to resolve technical challenges.
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.
Manage study deliverables and site payment targets while ensuring adherence to quality standards and procedural documents. Act as the primary liaison for functional leads to resolve risks, issues, and contract modifications.
The role focuses on optimizing inventory management and vendor relationships within Global Clinical Supplies operations. Key duties include analyzing demand requirements, managing purchase orders, and implementing continuous improvement initiatives.
The Biostatistician II implements statistical analysis plans for complex longitudinal registry data in autoimmune disease areas. They compile, analyze, and report statistical data to support research projects, pharmacovigilance, and registry coordination.
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.
Leads patient-centric medical writing projects focusing on Informed Consent Forms while managing timelines, budgets, and resources. Acts as a liaison between internal teams and clients to ensure high-quality, timely delivery of contractual deliverables.
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.
The CRA II 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.
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.
Provide administrative and financial support for processing payments to investigative sites while ensuring adherence to contractual guidelines and country regulations. Manage site relationships, resolve payment escalations, and train study teams on payment processes.
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 technical support, training, and product demonstrations for analytical and scientific solutions to optimize customer workflows. Collaborate with sales and R&D teams to drive business growth and ensure customer success across multiple technology platforms.
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.
The Account Manager will develop strategic sales plans and manage key relationships to increase revenue for scientific products and services. They will act as a trusted advisor, providing tailored solutions through a mix of virtual engagement and customer visits.
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.
Provide pre- and post-sales technical support and training for Orbitrap LC-MS instrumentation to proteomics customers. Develop technical content and present seminars to build customer advocacy and deepen scientific relationships.
Drive growth within health systems and laboratories by advancing the adoption of immunodiagnostic testing solutions. Orchestrate internal resources to expand testing menus and communicate clinical and economic value to senior executive stakeholders.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They act as a key country-level contact for regulatory activities and maintain accurate trial status information in tracking databases.
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-level contact for regulatory activities and maintain accurate trial status tracking.
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 role involves handling financial processes within the Recon and Project Delivery Team, including client accrual requests and BioA study reconciliations. The coordinator ensures data accuracy and maintains strong internal controls using various ERP systems.
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.
Lead high-visibility regulatory medical writing programs by managing client relationships, budgets, and project timelines. Ensure the quality and timely delivery of program documents while serving as a subject matter expert and risk escalation point.
The Safety Reporting Coordinator is responsible for preparing, reviewing, and submitting expedited and periodic safety reports for the APAC region, specifically Taiwan and Singapore. The role involves ensuring regulatory compliance, performing quality control, and collaborating with cross-functional teams to maintain safety reporting systems.
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.
Lead high-performing IT teams to drive innovation and digital transformation while overseeing critical infrastructure, security, and support services. Collaborate with business stakeholders to deliver strategic solutions that advance the company's mission in science and healthcare.
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.
Coordinate end-to-end planning and execution of high-profile international corporate events for customers and suppliers. Manage budgets, vendor relationships, and logistics to ensure seamless event delivery and high attendee satisfaction.
Create comprehensive documentation for complex scientific products and software platforms, including user guides and API documentation. Collaborate with cross-functional teams to translate technical information into user-friendly content and mentor junior technical communicators.
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.
Provide expert installation, maintenance, and repair services for sophisticated analytical and microscopy equipment. Resolve complex technical issues and train users to ensure optimal system performance across various research and industrial facilities.
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 update system documentation.
Provide expert-level technical support for customers using cell sorting and spectral flow cytometry technologies to optimize instrument performance. Collaborate with field teams and R&D to resolve complex hardware, software, and fluidics issues using remote diagnostic tools.
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.
Lead the North America Service Organization for the Chromatography and Mass Spectrometry Division, overseeing P&L delivery and organic growth. Drive operational excellence and customer allegiance through strategic leadership of field service, technical support, and service sales.
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.
Provide administrative and technical support for clinical trials, focusing on audit readiness, site activation, and eTMF maintenance. Coordinate feasibility assessments and maintain collaborative relationships with investigators and site personnel to ensure trial milestones are met.
Lead the enterprise-wide digital capability development strategy focusing on AI, automation, and data to democratize digital skills. Design and execute scalable learning programs and workshops to improve colleague productivity and accelerate digital transformation.
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.
Coordinates the preparation and regulatory approval of labels, patient cards, and dosing cards for clinical trials. Provides administrative support for clinical supplies operations across the study lifecycle.
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 manage the operations of the safety administration team, providing technical expertise and guidance to ensure operational excellence in patient safety. Oversee contracted safety services, manage project budgets, and lead global projects to ensure procedural and contractual compliance.
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.
Provide technical guidance on chemicals and promote a product portfolio to academic, pharmaceutical, and biotech customers. Deliver value propositions, conduct product demonstrations, and provide comprehensive application support to advance customer research.
Drive testing initiatives for generative AI and clinical trial technology using advanced manual testing practices. Lead test planning, execution, and defect management while mentoring junior engineers and collaborating with stakeholders.
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.
Lead a team of sales professionals to achieve forecast goals through strategic direction, coaching, and development. Manage district operations, maintain customer pipelines, and represent the company during sales calls and vendor relations.
The Senior CRA coordinates clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Responsibilities include conducting remote or on-site visits, managing documentation, and maintaining collaborative relationships with investigational sites.
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.
Coordinate and prepare local regulatory and ethics committee submissions in alignment with global strategies for clinical trials. Manage site-specific Informed Consent Forms and ensure all essential documents are collected and maintained in the TMF.
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.
Manage clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and company SOPs. Perform on-site and remote monitoring activities, including data verification and site relationship management.
The CRA II 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 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.
Draft, negotiate, and execute contracts and budgets with clinical study sites and principal investigators. Maintain professional relationships with sites while ensuring regulatory and financial risk mitigation.
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.
Perform and oversee day-to-day pharmacovigilance activities, including the collection, assessment, and tracking of safety information. Collaborate with project teams and clients to ensure operational excellence and compliance with regulatory timelines.
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.
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.
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.
Serve as the primary liaison for strategic accounts within the PPD Central Laboratory services model to drive growth and ensure delivery excellence. Lead governance models, manage high-impact issues, and partner with business development for account expansions.
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.
Lead the North America commercial growth agenda by developing multi-year strategies and managing a sales organization of over 50 members to hit $100M+ revenue targets. Act as a senior integrator across business units to align marketing, operations, and finance to improve customer allegiance and market share.
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.
Apply advanced analytics, machine learning, and AI techniques to solve complex business challenges across the enterprise. Develop and deploy sophisticated data science solutions to drive operational efficiencies and enhance decision-making.
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.
Lead global patient recruitment and retention strategies, overseeing the entire process from implementation to effectiveness. This includes managing third-party vendors, tracking enrollment metrics, and ensuring patient diversity requirements are met.
The Account Manager will develop strategic sales plans and manage key relationships with institutions like the Francis Crick and Southampton University to increase revenue. They will serve as a trusted advisor, providing tailored scientific solutions through a mix of virtual engagement and customer visits.
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.
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.
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 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.
Perform installation, maintenance, and repair of Molecular Analysis systems such as UV-Vis and FTIR Spectroscopy. Provide technical support and training to customers while coordinating service schedules and documenting field reports.
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 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.
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.
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 CRA Level II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation. They conduct remote and on-site visits to guarantee subject rights, data reliability, and audit readiness.
Provide advanced pre-sales and post-sales application support for Olink products to customers and distributors across South Korea and Southeast Asia. Collaborate with cross-functional teams to resolve technical issues and conduct training for core laboratories.
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.
Install, maintain, troubleshoot, and repair complex analytical and scientific instruments across research, industrial, and healthcare settings. Provide exceptional customer service and technical support to ensure equipment operational efficiency.
Manage the end-to-end supply chain for clinical trials to ensure timely distribution of materials and optimal inventory levels. Coordinate with cross-functional teams to develop study-specific plans and ensure compliance with GxP requirements.
The Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry Division products to Analytical Science and Scientific Research accounts. Key duties include driving revenue growth, managing customer relationships, and coordinating with technical specialists to provide tailored solutions.
Coordinate and prepare local regulatory submissions for Ministry of Health and Ethics Committees in alignment with global strategies. Manage site start-up activities and maintain trial status information in tracking databases to ensure timely site activation.
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.
Serve as a strategic partner to business leaders to identify performance gaps and develop targeted learning strategies. Collaborate with the Design & Development team to implement solutions that drive measurable business outcomes and sustained behavior change.
Manage full-cycle recruitment for diverse roles across business units as a strategic talent advisor. Collaborate with hiring managers to develop sourcing strategies and build strong talent pipelines while ensuring an outstanding candidate experience.
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.
Define and govern the technical blueprint for enterprise AI and data ecosystems, focusing on scalability, security, and alignment with enterprise standards. Lead the design of GenAI patterns, data platforms, and governance frameworks while partnering with leadership on long-term strategy.
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 X-ray photoelectron spectrometers. Collaborate with sales teams to plan equipment layouts and provide technical support to customers.
Perform periodic maintenance, troubleshooting, and installation of electron microscopes and analytical devices. Collaborate with sales teams to plan equipment layouts and specifications for customer sites.
Oversee, train, and performance manage a team of clinical operations staff using metrics and KPIs. Ensure adherence to SOPs and WPDs while collaborating with leadership on resourcing and strategic planning.
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.
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.
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 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.
Provides senior administrative and financial support for processing payments to FSP investigative sites, including budget entry and reconciliations. Responsible for ensuring adherence to contractual guidelines and mentoring junior team members.
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 Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry Division products while maintaining long-term customer relationships. The role involves identifying new client opportunities, driving revenue growth, and coordinating with technical specialists to provide expert solutions.
Execute manual test cases for functional, regression, and integration testing to ensure high-quality software delivery. Identify and track defects while collaborating with developers to resolve issues and maintaining comprehensive test documentation.
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.
The Account Manager is responsible for driving revenue growth by developing strategic relationships with customers and promoting a portfolio of scientific products. The role involves implementing sales strategies and identifying new business opportunities to help customers achieve their goals.
Conduct remote and on-site monitoring visits to ensure clinical trials are performed according to protocols, ICH-GCP guidelines, and regulatory requirements. Manage site documentation, assess investigational product inventory, and maintain collaborative relationships with investigative sites.
Drive sales growth and customer engagement as the technical expert for the HPLC portfolio across Germany. Provide technical consultation, conduct product demonstrations, and collaborate with cross-functional teams to optimize customer chromatography workflows.
Responsible for planning and delivering signal detection and product safety activities to ensure patient safety. This includes synthesizing data from multiple sources into insights and collaborating with stakeholders to establish safety evidence platforms.
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.
Responsible for the strategic and operational leadership of the PDX business across Germany, Austria, and Switzerland. This includes leading the regional sales organization, driving sustainable revenue growth, and managing strategic key accounts.
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.
Drive test volume growth for BRAHMS Procalcitonin (PCT) by engaging clinical and financial stakeholders at hospitals. Develop and implement hospital-wide protocols for sepsis and lower respiratory tract infection management.
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.
Implement strategic sales initiatives to drive business growth and achieve targets within the assigned territory. Manage customer relationships, leverage technical expertise in molecular biology, and optimize sales strategies to accelerate performance.
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.
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.
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.
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.
Ensure international trade operations comply with regulatory requirements through policy implementation and transaction monitoring. Manage day-to-day export activities including classification, screening, and licensing while collaborating with internal stakeholders and freight forwarders.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage strategic accounts and build executive-level relationships to position the company as a preferred provider.
Perform installation, maintenance, and repair of sophisticated analytical and microscopy equipment at customer sites. Provide technical support, train users on equipment operation, and collaborate with internal teams to resolve complex system issues.
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.
The CRA II 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 clinical sites.
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 audit readiness.
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.
Define and implement global policies for contamination control, sterility assurance, and microbiology across all PSG sites. Provide subject matter expertise to support site-based teams with risk assessments, deviation investigations, and facility design.
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.
The CRA I is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing essential documentation. They conduct remote and on-site visits to verify data accuracy and maintain collaborative relationships with clinical sites.
Design, develop, and maintain HL7 interfaces and integrations between clinical systems and EHR/EMR platforms. Ensure secure, compliant data exchange while troubleshooting interface issues and managing integration engines.
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.
Identify new business opportunities and develop strategic partnerships to drive growth across multiple divisions and regions. Analyze market trends and create comprehensive business plans to expand market presence in the scientific community.
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.
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.
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.
Lead a technical development support team focused on troubleshooting, root cause analysis, and operational stability for digital data and integration platforms. Ensure all code changes comply with SDLC, validation, and change control processes within a regulated environment.
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.
The role involves preparing and coordinating country-specific regulatory and ethics committee submissions in alignment with global strategies. It also includes managing site start-up activities, maintaining trial status databases, and ensuring compliance with SOPs.
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.
The Clinical Sales Specialist supports growth through technical sales expertise, customer relationship management, and the delivery of effective value propositions. Responsibilities include conducting product demonstrations, providing application support, and managing strategic sales activities and business reviews.
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.
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.
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.
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.
Provide administrative and technical support for clinical trials, focusing on audit readiness, site activation, and eTMF maintenance. Coordinate feasibility assessments and maintain collaborative relationships with investigators and site personnel.
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 Regulatory Affairs Scientist will provide technical oversight for regulatory submissions and manage compliance reporting. They will also develop training on chemical compliance standards and support policy implementation.
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.
Lead and execute non-CRF external data acquisition across the setup, conduct, and closeout phases of multiple clinical studies. Act as the primary liaison between clients and internal departments to ensure accurate and timely ingestion of external data into repositories.
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 Safety Specialist is responsible for driving profitable sales growth for the safety portfolio within the assigned Quebec territory. They will build strong customer relationships, provide tailored solutions, and collaborate with internal teams to meet operational and compliance needs.
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 role involves driving growth by identifying and converting new business opportunities within the semiconductor industry while building relationships with key decision-makers. You will align Thermo Fisher Scientific solutions with customer roadmaps and collaborate across divisions to deliver comprehensive, high-value technical solutions.
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 Senior Enterprise Project Manager independently leads a portfolio of complex client projects end-to-end within client services, focusing on maintaining client relationships and ensuring an excellent customer experience throughout the Clinical Trial Services journey. Key duties include leading large project portfolios, improving organizational processes and tools, providing mentorship, and acting as the single point of escalation for client projects.
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 Strategic Account Manager is responsible for maintaining reagent revenue within a prescribed group of laboratory accounts in the ImmunoDiagnostics Division, focusing on retaining and growing existing business in Reference, Hospital, and Health System Laboratories. This role involves developing and executing retention strategies for Autoimmunity and Allergy accounts, holding Customer Business Reviews, and acting as the primary liaison between the customer and IDD Commercial personnel where growth opportunities exist.
The specialist will act as a subject matter expert to design, develop, deliver, and improve products, programs, and services aimed at optimizing processes, behaviors, performance, and audit readiness within the Clinical Research Group. Key duties involve collaborating on initiatives to ensure quality operational delivery through efficient processes, systems, training, and communications, while also leading process improvement efforts.
The Senior Country Approval Specialist manages the preparation, review, and coordination of Country Submissions, aligning with the global submission strategy. This role involves providing local regulatory strategy advice and serving as the primary contact for investigators and local regulatory authorities to ensure timely submission management.
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 Clinical Research Associate will thrive in multi-national project teams, focusing on delivering exemplary customer service across challenging projects. Responsibilities include performing and coordinating all aspects of the clinical monitoring process, with the qualification to conduct monitoring activities independently.
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.
