The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements and investigator grant budgets. They ensure compliance with company and client processes while managing risks and coordinating with internal teams to meet site activation timelines.
The Senior Technical Sales Specialist will drive revenue growth and customer success by applying technical expertise to identify opportunities and build strong client relationships. They will provide technical leadership, conduct product demonstrations, and act as a trusted advisor to help customers achieve their research and development goals.
The Lead DevOps Engineer will spearhead CI/CD strategy, infrastructure as code, and system performance optimization to support agile development. They will also manage container orchestration platforms and mentor junior engineers to ensure operational success.
The Project Manager provides tactical support for client-facing projects, focusing on financial management and logistical coordination for clinical trials. They are responsible for reviewing sample documentation, managing database imports, and ensuring compliance with quality assurance procedures.
The Data Reviewer ensures the integrity and quality of laboratory and chromatographic data by verifying compliance with analytical methods, SOPs, and GMP standards. They communicate findings to laboratory staff, prepare QC statements, and support process improvement initiatives.
The Senior Clinical Data Team Lead acts as a primary liaison for clinical data management activities across complex projects. They are responsible for monitoring study metrics, managing project budgets, and mentoring junior staff to ensure operational excellence.
The Project Manager will oversee the end-to-end supply chain for clinical trials to ensure timely distribution and inventory optimization. They will also collaborate with cross-functional teams, mentor junior staff, and represent the department in strategic initiatives.
The Clinical Data Team Lead acts as the primary data manager for clinical studies, overseeing data management activities and ensuring operational excellence. They serve as a liaison between the project team and clients, while also mentoring junior staff and managing project documentation and metrics.
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 Assistant Clinical Research Associate provides remote support for site preparedness, monitoring processes, and study management tasks. They coordinate site activities, manage essential documents, and perform data reconciliation in accordance with regulatory guidelines.
The Account Director is responsible for acquiring and retaining high-value clients within the small and mid-sized pharmaceutical market. They will manage the entire sales process, including lead generation, proposal development, and negotiation to meet annual sales targets.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, maintain study documentation, and ensure compliance with regulatory standards and project protocols.
The Senior Manager will lead a team of clinical data management staff, overseeing performance, professional development, and project resourcing. They will ensure all clinical trial tasks are completed accurately, on time, and within budget while maintaining compliance with regulatory guidelines.
The Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They must provide exceptional customer service while ensuring all work adheres to safety protocols and quality standards.
The Site Payments Associate II is responsible for managing and processing patient payments for clinical trials. They ensure accurate and timely financial transactions in accordance with study protocols and site agreements.
The Principal Medical Writer is responsible for planning, coordinating, and delivering high-quality clinical and scientific documents such as IBs, INDs, and MAAs. They also provide senior-level review, mentorship to junior staff, and support project management activities to ensure operational excellence.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They oversee clinical monitoring, regulatory submissions, and team coordination to ensure compliance with study protocols and corporate policies.
The Senior Director will set global strategy and drive profitable growth across the OEM and Advanced Therapeutics commercial businesses. This role involves leading a global organization, managing key strategic accounts, and fostering cross-functional collaboration to execute consistent go-to-market approaches.
The Senior Validation Specialist will implement, configure, and support LIMS products while managing computer system validation documentation and testing. They will also lead validation activities, resolve complex technical issues, and collaborate with cross-functional teams to ensure compliance with regulatory standards.
The Safety Committee Administrator provides project coordination and safety support for global clinical programs, specifically focusing on DSMB and EAC committees. Responsibilities include managing member contracts, facilitating meetings, drafting minutes, and ensuring all program files remain audit-ready.
Provide medical leadership to study teams, including protocol development, site selection, and real-time medical monitoring of clinical trials. Ensure medical validity, subject safety, and regulatory compliance while collaborating with cross-functional teams to deliver high-quality study data.
The Senior Project Manager serves as the primary contact for sponsors and is accountable for the overall delivery of pregnancy registry projects regarding quality, time, and cost. They lead cross-functional teams, manage project budgets, and ensure compliance with regulatory requirements and internal SOPs.
Lead patient-centric medical writing projects with a focus on Informed Consent Forms while managing timelines, budgets, and resources. Collaborate with cross-functional teams and clients to ensure high-quality deliverables and resolve project risks.
The Senior Director will define and execute the commercial strategy for the EMEA Clinical Sequencing business to achieve revenue and profitability targets. They will lead a diverse team, manage strategic customer relationships, and collaborate across divisions to drive market growth and operational excellence.
The Senior Manager will lead technology initiatives and digital transformation projects while ensuring regulatory compliance and audit readiness. They will partner with business leaders to develop strategic technology roadmaps and manage cross-functional teams across multiple locations.
The Manager leads a global team in designing, building, and supporting secure, scalable integrations across enterprise applications and cloud platforms. They are responsible for setting engineering standards, mentoring staff, and ensuring operational excellence through automation and modern DevOps practices.
The Business Transformation Analyst will support the accuracy and integrity of laboratory database content by performing technical reviews and implementing approved updates. This role involves collaborating with global stakeholders to ensure compliance with SOPs and contributing to process improvement initiatives.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Responsibilities include conducting site visits, verifying data accuracy, managing documentation, and resolving site-related issues to ensure subject safety and data reliability.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring and issue resolution.
The Senior Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of clinical study sites to ensure compliance with international guidelines and company procedures. They act as the primary contact for study sites, driving performance, managing supplies, and ensuring data quality through regular monitoring visits and risk assessments.
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 financial stewardship, and ensure compliance with regulatory requirements and internal SOPs.
You will serve as a strategic talent advisor managing full-cycle recruitment for diverse roles across business units. This involves collaborating with hiring managers to develop sourcing strategies, build talent pipelines, and deliver an outstanding candidate experience.
You will drive growth and adoption of the molecular diagnostics portfolio by identifying market opportunities and developing evidence-based expansion strategies. Additionally, you will lead integrated marketing campaigns and create clinical education content to support global revenue targets.
You will drive revenue growth and customer success by providing technical sales expertise for scientific instruments and solutions. You will also manage key accounts and collaborate with cross-functional teams to implement effective sales strategies.
The Senior Biostatistician serves as the statistical lead on high-profile client projects, designing studies and developing statistical analysis plans. They provide strategic leadership to ensure high-quality real-world evidence generation while collaborating with cross-functional teams.
The Business Intelligence Analyst will support sales execution, data visibility, and operational efficiency by managing quota workbooks and commercial reporting solutions. They will analyze complex data sets and develop actionable insights to drive business growth and support sales compensation programs.
You will identify and pursue new business opportunities while developing strategic relationships with key accounts to drive growth. Additionally, you will collaborate across divisions to deliver comprehensive solutions and manage the sales pipeline through the CRM system.
The Compliance Manager provides clinical quality oversight and acts as a single point of contact for client partners to ensure consistent quality culture. They are responsible for facilitating quality risk management, analyzing key quality indicators, and driving support for partnership governance.
Serve as a primary scientific liaison between the company and laboratory customers to provide clinical education and support. Develop and maintain relationships with key opinion leaders and stakeholders to drive scientific partnerships and product adoption.
Leads a team providing specialized demand and supply planning services to clinical trial clients to ensure optimal inventory and patient supply. Develops and monitors performance metrics while integrating forecast data into the divisional S&OP process to drive operational efficiency.
The Senior ICF Project Manager will lead patient-centric medical writing projects, specifically focusing on Informed Consent Forms (ICFs) through collaboration with internal and client teams. They are responsible for managing project timelines, budgets, resources, and ensuring the quality and timely delivery of all project documentation.
The Associate Financial Systems Analyst will support the administration, maintenance, and continuous improvement of Oracle Cloud ERP and related financial applications. They will collaborate with global stakeholders to troubleshoot issues, document requirements, and assist in the implementation of financial modules.
Develop and execute strategic sales plans to drive revenue growth and maximize business within assigned global key accounts. Build and maintain strong relationships with senior-level clients while leading the RFP and RFI processes to secure new business opportunities.
The Business Development Associate will identify and qualify new business opportunities within the biotech and pharmaceutical sectors for GMP analytical services. They will manage client relationships, coordinate account setups, and collaborate with internal teams to submit proposals and drive revenue growth.
The Senior Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage project budgets, and ensure compliance with regulatory requirements and internal SOPs.
Provide expert installation, maintenance, and repair services for analytical and microscopy equipment across the Nordic region. Manage customer relationships, perform system certifications, and train users to ensure optimal performance of laboratory systems.
The Quality Manager is responsible for the operational execution of the Pharmacovigilance Quality Management System and driving continuous improvement within the Global Patient Safety area. Key duties include managing audit and inspection readiness, overseeing CAPA activities, and maintaining procedural documentation and training programs.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct remote or on-site visits to assess regulatory adherence and manage essential documentation throughout the clinical trial lifecycle.
The Senior CRA coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage documentation, and facilitate communication between investigative sites and project teams.
You will drive growth and adoption of the molecular diagnostics portfolio by creating market expansion strategies and evidence-based adoption frameworks. Additionally, you will lead integrated marketing campaigns and develop compelling content to translate complex clinical value into actionable demand generation programs.
The BioProduction Sales Specialist will drive growth and develop new business opportunities across the BioProduction portfolio within assigned accounts. They will manage primary customer relationships and coordinate with technical and applications teams to deliver comprehensive bioprocess solutions.
The Senior Medical Writer serves as the primary author for clinical study reports, protocols, and regulatory documents while ensuring high-quality scientific communication. They also provide mentorship to junior staff and assist in program management activities such as budget and timeline development.
The Biostatistician II functions as a lead statistician responsible for statistical analysis, database creation, and the development of statistical analysis plans. They also lead project teams, manage budgets, and provide mentorship to junior staff members.
The Senior Project Manager leads a portfolio of projects, acting as the primary operational interface between the client and the laboratory. They are responsible for overseeing project performance, managing budgets, and ensuring compliance with regulatory guidelines and internal SOPs.
The Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct remote or on-site visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
The Global Project Manager oversees the implementation and execution of home visits for clinical trials by coordinating with clients, internal teams, and external vendors. They are responsible for developing study-specific plans, ensuring regulatory compliance, and mentoring junior team members.
The Medical Director provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. They also manage safety variables, provide medical consultation to project teams, and assist in the review of clinical study reports and safety data.
The Account Executive is responsible for selling consumable and diagnostic lab supplies and instrumentation within a defined territory. They will manage strategic direction, maintain customer relations, and develop sales opportunities to meet or exceed sales objectives.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet project timelines.
The Senior Regulatory Affairs Specialist will provide strategic regulatory intelligence and guidance to support product development from preclinical stages through registration. They will also prepare and review regulatory submissions while acting as a liaison between internal teams and external clients.
Perform on-site installation, maintenance, and repairs of electron microscopes while providing technical support to customers. Coordinate work schedules and provide accurate service reports to ensure high levels of customer satisfaction.
Serve as a technical expert and consultant to support bioprocessing customers with process development, optimization, and technology integration. Lead pre- and post-sales technical activities while capturing customer insights to influence product roadmaps and innovation.
The Associate Director provides operational leadership for clinical operations within a client-aligned portfolio, ensuring effective execution of deliverables and proactive risk management. They are responsible for coaching teams, managing resources, and maintaining strong relationships with client stakeholders to meet project and financial objectives.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including document collection, system updates, and remote monitoring tasks. They assist in coordinating study activities, maintaining vendor trackers, and ensuring compliance with regulatory guidelines and SOPs.
The PV Project Delivery Manager coordinates and oversees contracted pharmacovigilance deliverables across multiple services while ensuring project financial health and compliance. They serve as the primary point of contact for clients, driving project timelines and managing risk mitigation strategies.
The Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They will provide exceptional customer service and support while ensuring adherence to safety and quality standards in various laboratory environments.
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They manage site processes, document observations, and facilitate communication between the sponsor and investigative sites throughout the clinical trial lifecycle.
The Account Manager will represent the company and manage the full sales process from pre- to after-sales support for molecular spectroscopy products. They are responsible for building long-term customer relationships, conducting product presentations, and managing sales opportunities within the assigned territory.
The Clinical Research Associate ensures clinical studies are conducted in compliance with protocols, ICH-GCP, and local regulatory requirements. They are responsible for coordinating all aspects of the clinical monitoring process and ensuring the accuracy and integrity of study data.
The 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 Sr Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and subject safety through risk-based monitoring. They will also manage site documentation, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial process.
The Application Administrator provides L2 operational support for the Clarity PPM platform, including incident resolution, application monitoring, and data-integrity checks. The role also involves managing user access, supporting deployments, and maintaining operational documentation in compliance with SOX standards.
The Senior Systems Developer serves as the technical lead for the Clarity PPM platform, providing L3 support and managing complex development, configuration, and integrations. They are responsible for resolving production issues, leading root-cause analysis, and ensuring technical standards are met across the support team.
The Application Administrator provides L2 operational support for the Clarity PPM platform, including incident resolution, service requests, and application monitoring. The role also involves maintaining system health, performing data-integrity checks, and supporting configuration and deployment activities.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform on-site and remote monitoring visits, manage documentation, and facilitate communication between investigative sites and project teams.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
The CRA performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct remote or on-site visits, manage documentation, and maintain collaborative relationships with investigational sites.
Performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. Conducts risk-based monitoring, manages essential documentation, and facilitates communication between investigative sites and the project team.
The Clinical Trial Coordinator II provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage trial documentation, perform file reviews, and maintain communication with investigators and internal departments to meet project timelines.
The Global Project Manager oversees the implementation and execution of home visits within clinical trial protocols. This role involves coordinating with internal teams, clients, and vendors while ensuring compliance with local regulations.
The Senior Medical Writer will serve as a primary author for complex clinical and regulatory documents, ensuring they meet industry standards and regulatory guidelines. They will also collaborate with cross-functional teams and provide mentorship to junior staff to ensure high-quality deliverables.
You will lead statistical tasks throughout the full clinical trial process, including study design, protocol writing, and final analysis. The role involves collaborating with clients and regulatory authorities to advance life-changing therapies.
The role involves leading due diligence proposals for operational pursuits, including restructuring and capital expenditures. You will collaborate with executive leadership to analyze operational performance, financial models, and risks to support strategic decision-making.
The Country Approval Associate supports the preparation, review, and coordination of regulatory and ethical submissions in alignment with global strategies. They also assist with site start-up activities, budget negotiations, and the maintenance of trial status databases.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating investigator grant budgets and contractual terms with study sites. They coordinate with internal teams to ensure site startup activities align with contractual timelines and established risk management processes.
The associate will draft, review, and negotiate clinical trial site contracts and budgets while ensuring compliance with internal and client processes. They will also coordinate with internal functional departments to align site startup activities with contractual timelines.
The Account Executive will drive revenue growth and build lasting customer relationships by representing a portfolio of scientific products and services. They are responsible for prospecting new business, managing key accounts, and executing strategic sales plans within the assigned territory.
The Senior Site Contract Specialist manages the preparation, negotiation, and finalization of investigator contracts while ensuring compliance with budgetary and legal guidelines. They also liaise with internal functional teams and sites to align startup activities with critical path timelines.
The Senior Research Associate will lead the design and implementation of data collection projects while providing scientific guidance and managing project deliverables. They will also engage with clients, manage project budgets and timelines, and contribute to business development activities.
Provide scientific expertise, application support, and training for the Luminex and Immunoassay portfolio to customers across the EMEA region. Partner with sales teams to deliver pre- and post-sales support while effectively resolving technical customer escalations.
The Principal Regulatory Affairs Specialist provides regulatory advice and manages global regulatory submissions while acting as a liaison between project teams and health authorities. They are responsible for assessing regulatory documents, performing quality control on submission packages, and ensuring strategic alignment across projects.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and procedural documents. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring and issue resolution.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and company procedures. They act as the primary contact for study sites, driving performance and ensuring data quality throughout the study lifecycle.
The Clinical Trial Manager leads local study teams to ensure clinical studies are delivered on time, within budget, and in compliance with international guidelines and local regulations. They are responsible for site selection, monitoring activities, regulatory submissions, and maintaining high-quality data throughout the study lifecycle.
Lead local study teams to deliver clinical studies in compliance with international guidelines, budget, and timelines. Oversee site selection, monitoring activities, and regulatory documentation to ensure high-quality data delivery.
The Project Manager III will lead end-to-end commercial projects, ensuring they are delivered within scope and budget while meeting business objectives. They are responsible for developing project plans, managing cross-functional teams, and reporting progress to leadership.
The Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements while ensuring compliance with budgetary and legal parameters. They will coordinate with internal teams to align site startup activities and manage risk throughout the contract lifecycle.
The Key Account Executive is responsible for driving organic growth within strategic accounts by increasing share of wallet and expanding solution adoption. They serve as a trusted advisor to customers, aligning business objectives with enterprise solutions while coordinating cross-functional resources.
Manage the end-to-end supply chain for clinical trials to ensure timely distribution of materials and maintain optimal inventory levels. Collaborate with cross-functional teams to integrate supply chain activities with project logistics strategies and regulatory compliance.
The Country Approval Associate supports the preparation, review, and coordination of country submissions in alignment with global strategies. They also manage site start-up activities, maintain trial status databases, and ensure regulatory compliance for clinical study documentation.
The Senior Clinical Data Team Lead acts as a primary liaison for clinical data management activities, overseeing project budgets, timelines, and study metrics. They are responsible for leading complex studies, delegating tasks, and mentoring junior staff to ensure operational excellence.
The Associate Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice, support site start-up activities, and maintain accurate trial status information in tracking databases.
Manage contract processes, documentation, and administration while collaborating with internal stakeholders to ensure smooth commercial operations. Coordinate with Account Managers and Legal teams to facilitate timely contract execution and maintain compliance with corporate policies.
The Fleet Administrator manages company car contracts, coordinates with leasing suppliers, and supports colleagues with vehicle inquiries via a case management system. They are also responsible for maintaining accurate fleet records, ensuring data compliance, and facilitating the full lifecycle of company car allocations.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, perform file reviews, and maintain clinical trial databases while ensuring compliance with SOPs and regulatory guidelines.
You will lead the PDX sales team in Austria and Switzerland while managing your own sales territory and key accounts. The role involves driving commercial growth, implementing regional sales strategies, and fostering a performance-oriented culture through data-driven decision-making.
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 Global Project Coordinator manages supply readiness for home care visits and coordinates onboarding and training for healthcare professionals. They act as a primary liaison between clinical sites, vendors, and internal teams to ensure the operational success of decentralized clinical trials.
The Product Specialist will market controlled environment products within a designated territory to exceed sales forecasts and growth targets. They will collaborate with Laboratory Equipment Representatives to identify sales opportunities and maintain accurate CRM funnel reports.
The Principal Programmer Analyst provides strategic technical and validation leadership for complex Pharmacovigilance systems and initiatives. They ensure systems remain compliant, inspection-ready, and aligned with business objectives while driving process automation and continuous improvement.
Lead Talent Acquisition projects from ideation to execution, focusing on digital solutions, custom app design, and agentic system deployment. Consult with stakeholders to evaluate recruitment processes and recommend strategic improvements to enhance efficiency and user experience.
The Senior Regulatory Affairs Specialist acts as a liaison between project teams and health authorities to manage regulatory strategy and submission activities. They are responsible for the assessment of regulatory documents, preparation of global submissions, and ensuring quality control of final submission packages.
The Associate Director provides operational leadership for clinical operations within a client-aligned portfolio, ensuring effective execution of deliverables and proactive risk management. They are responsible for building strong client relationships, managing resources, and coaching teams to meet project and portfolio objectives.
The Field Service Technician is responsible for performing maintenance, repairs, and equipment qualifications for customers within the Hamburg region. This role involves managing a personal spare parts inventory, documenting system activities, and providing technical consultation to customers.
The Associate Investigator Grant Analyst prepares, reviews, and finalizes global investigator grant budgets and payment schedules for clinical studies. They also liaise with clients and internal teams to negotiate budget parameters and ensure site startup activities align with project timelines.
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 represent the company at professional meetings to meet annual growth targets.
Lead a sales team to drive revenue growth and market expansion for laboratory consumables and chemicals. Develop and implement strategic sales initiatives while fostering strong customer partnerships across a matrix organization.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Facilitates communication between investigative sites and project teams while managing trial documentation and site status reporting.
Monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. Facilitates communication between investigative sites, clients, and internal teams while managing trial documentation and site progress.
The 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 documentation and trial progress to ensure audit readiness.
Lead and develop an international team of eight sales professionals to drive revenue growth and profitability across the EMEA region. Build and strengthen strategic OEM customer relationships while collaborating with internal stakeholders to ensure effective delivery and resolve commercial challenges.
The Operational Bid Specialist supports financial and business objectives by leading and developing high-quality, customer-focused clinical supply proposals. They collaborate with internal teams and subject matter experts to evaluate RFPs, define bid strategies, and ensure accurate budget mapping.
The Account Manager will support revenue growth and manage strategic relationships within the New Hampshire, Maine, and Boston markets. They will implement sales strategies, identify new business opportunities, and provide technical support for scientific product portfolios.
The Account Manager III will develop and implement strategic sales plans while managing key account relationships to drive revenue. They will work with cross-functional teams to provide tailored scientific solutions and ensure customer satisfaction through consultative engagement.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They will conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
The Senior Project Coordinator provides administrative and technical support to the Global Clinical Supplies team by managing project documentation, regulatory records, and data repositories. They also assist in project planning, coordinate team communications, and mentor junior staff to ensure compliance with GCP and project timelines.
The 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, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
The Senior Manager will drive commercial growth and market penetration across LATAM (excluding Brazil) by developing regional strategies and managing distributor networks. They will also lead business development efforts, maintain key stakeholder relationships, and provide accurate sales forecasting and market analytics.
The Manager of Clinical Operations oversees, trains, and mentors a team while utilizing metrics and KPIs to ensure project performance and adherence to SOPs. They also collaborate with leadership on resourcing, business development, and process improvement initiatives.
The Local Clinical Trial Manager leads the local study team and serves as the primary operational point-of-contact for clinical trial delivery within the country. They are accountable for ensuring clinical deliverables meet time, budget, and quality expectations while maintaining compliance with regulatory and internal standards.
The Principal Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities while ensuring site start-up activities meet critical path timelines.
The Regulatory Project Manager will lead strategic regulatory initiatives and ensure global compliance across medical devices, pharmaceuticals, and biologics. They will collaborate with cross-functional teams to manage product development, regulatory submissions, and lifecycle management.
Lead and develop a high-performing Site Payments team to ensure accurate, compliant, and timely investigator payments across clinical trials. Drive operational excellence by managing project delivery, mitigating risks, and implementing process improvements in collaboration with senior leadership.
The Medical Director provides medical leadership for clinical trials, including protocol development, site selection, and real-time medical monitoring to ensure subject safety. They serve as the primary medical liaison between the sponsor and internal departments while ensuring compliance with regulatory guidelines and SOPs.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory requirements.
You will supervise technical support staff across IT disciplines including Desktop Services and Network Communications. You will drive service excellence through cross-functional partnerships while implementing technical solutions to meet business needs.
The Director will lead the vision, strategy, and lifecycle of a global portfolio of AI-enabled products for medical writing and clinical development. This role involves managing cross-functional teams, defining product roadmaps, and ensuring regulatory compliance and quality across all clinical document workflows.
The Field Service Engineer performs onsite installations, repairs, and preventative maintenance on laboratory instruments within an assigned territory. They also interact with customers to resolve technical issues, identify improvement areas, and promote service contracts.
The Principal Regulatory Affairs Professional provides strategic regulatory guidance and intelligence to support product development from preclinical stages through registration. They also lead project teams, ensure compliance with global regulatory requirements, and act as a primary liaison for internal and external clients.
The Clinical Team Manager is responsible for achieving clinical deliverables within contractual time, quality, and cost expectations. They manage clinical operational aspects, lead teams, and ensure compliance with ICH GCP and study protocols.
Leads study planning and portfolio scheduling across multiple clinical research units to ensure accurate, executable study placement. Coordinates cross-functionally with site leadership, investigators, and operational teams to optimize capacity and manage scheduling risks.
Design and implement inventory management plans to forecast supply for global clinical trials while optimizing supply chain strategies. Collaborate with cross-functional teams and clients to manage project budgets, IRT settings, and ensure continuity of subject supply.
Develop and execute strategic sales plans to drive revenue growth and expand market share within assigned global biotech accounts. Build and maintain strong relationships with key client stakeholders while leading the RFP and RFI processes to secure new business opportunities.
The Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of allocated studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, develop study tools, and ensure compliance with ICH GCP and regulatory requirements throughout the trial lifecycle.
The Clinical Research Associate coordinates all aspects of the clinical monitoring and site management process to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
Manages the complete life cycle of translation projects, including planning, scheduling, and risk management. Facilitates communication within the project team and maintains day-to-day relationships with clients.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also manage study documentation, facilitate cross-functional communication, and assist with process improvements and staff training.
You will serve as a technical expert providing comprehensive support, training, and troubleshooting for advanced scientific instrumentation. Additionally, you will collaborate with sales and R&D teams to optimize applications and drive business growth through customer engagement.
The Field Service Engineer will provide expert installation, maintenance, troubleshooting, and repair services for advanced analytical equipment. They will also manage service activities, provide user training, and collaborate with global teams to ensure optimal system performance.
The position is responsible for securing revenue objectives for allergy and autoimmune products by prospecting and closing new business within a designated geographic territory. The role involves managing existing laboratory accounts and collaborating with internal divisions to drive clinical adoption and long-term growth.
Manage contract processes, documentation, and administration while collaborating with internal stakeholders to ensure smooth commercial operations. Coordinate with Account Managers and Legal teams to facilitate timely contract execution and ensure compliance with corporate policies.
Develop and grow the Bioproduction market in Denmark by managing the entire portfolio and implementing strategic sales plans. Collaborate with internal teams and field applications to drive sales objectives and provide technical support to key biopharmaceutical accounts.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between sites and the project team.
The Marketing Manager will lead the U.S. go-to-market strategy for the allergy product portfolio, driving product adoption and utilization through effective marketing tactics. They will also manage sales enablement initiatives and conceptualize digital campaigns to educate healthcare providers and laboratorians.
Perform on-site installation, preventive maintenance, and repair support for chromatography and mass spectrometry equipment at customer laboratories. Train customers on equipment operation and provide effective communication between the customer and the company.
The Associate Director manages a team of clinical staff across multiple countries to ensure clinical deliverables meet quality, time, and cost expectations. They are responsible for project oversight, financial management, staff development, and driving cross-functional initiatives to achieve business objectives.
Provide onsite service, including repairs, preventive maintenance, and installation of IDD analyzers at customer sites. Collaborate with internal partners and provide technical training to biomedical technicians and operators.
The Senior Account Manager is responsible for driving sales and supporting the Chromatography and Mass Spectrometry Division portfolio within the assigned territory. This role involves developing strategic growth plans, managing customer relationships, and leading cross-functional teams to solve complex scientific challenges.
You will coordinate clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. This includes conducting site visits, verifying data accuracy, and managing documentation to guarantee subject rights and data reliability.
The Label Designer will develop and implement efficient labeling solutions while ensuring compliance with GMP and regulatory standards. The role involves collaborating with cross-functional teams to optimize labeling processes and maintain technical documentation.
The Senior Research Associate will lead scientific coordination and project management for de novo data collection projects, including drafting protocols and reports. They will also engage with clients, manage project budgets and timelines, and contribute to business development activities.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
The Field Applications Scientist serves as a technical advisor to help customers optimize the use of advanced technologies through demonstrations, training, and troubleshooting. They collaborate with sales teams to provide pre-sales and post-sales support while building long-term customer relationships.
The Field Service Engineer will install, maintain, troubleshoot, and repair complex analytical and scientific instruments across research, industrial, and healthcare settings. They are responsible for providing exceptional technical support, training customers on equipment operation, and documenting all service activities accurately.
The Account Manager will maintain and grow the Allergy and Autoimmune market by managing customer accounts and developing strong relationships across the assigned territory. Responsibilities include negotiating contracts, managing tenders, and collaborating with internal teams to ensure accurate forecasting and account planning.
The Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry products while maintaining long-term customer relationships. They will identify new client opportunities, negotiate contracts, and lead commercial activities within their assigned territory.
The Field Service Engineer will conduct on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and maintain detailed service reports while acting as a subject matter expert.
The Country Approval Specialist manages, reviews, and coordinates local regulatory submissions to ensure alignment with global submission strategies. They also provide regulatory advice to internal clients and coordinate site start-up activities to meet critical project timelines.
The Sr. Manager, Strategic Key Accounts is responsible for managing and expanding relationships with key customers in the global in vitro diagnostics market. This role involves leading commercial negotiations, developing strategic account plans, and coordinating cross-functional teams to drive revenue growth.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence, manage documentation, and resolve site-related issues.
The Senior Portfolio Manager is responsible for the strategic and commercial management of a clinical diagnostics portfolio, including supplier relationship management and driving profitable growth. They will lead business reviews, negotiate commercial terms, and collaborate across internal teams to execute product launches and marketing initiatives.
The Field Service Engineer II is responsible for installing, maintaining, and repairing sophisticated analytical and scientific instrumentation at customer sites. They provide technical support, perform preventive maintenance, and ensure high levels of customer satisfaction through effective troubleshooting and communication.
The Sr. Manager, Strategic Key Accounts is responsible for managing and expanding relationships with key customers in the global in vitro diagnostics market. This role involves developing strategic account plans, leading commercial negotiations, and coordinating cross-functional teams to drive revenue and portfolio growth.
The Vendor Management Coordinator oversees clinical supply operations, including vendor coordination, purchase order management, and invoice reconciliation. They ensure all activities comply with company policies, GxP regulations, and project timelines while maintaining effective communication with internal stakeholders.
The Senior Clinical Trial Coordinator provides administrative and technical support to project teams while facilitating project activities and serving as a cross-functional liaison. They are responsible for maintaining study documentation, performing file reviews, and ensuring project tasks are completed on time and within budget.
The Clinical Trial Coordinator II provides administrative and technical support to project teams by facilitating project activities and acting as a cross-functional liaison. They are responsible for maintaining study documentation, performing file reviews, and ensuring tasks are completed on time and within budget.
The Country Approval Associate manages and coordinates local regulatory submissions and site start-up activities in alignment with global strategies. They act as a key contact for regulatory and ethical submission-related activities while ensuring compliance with internal and client SOPs.
The Site Compliance Lead manages the site compliance team to ensure adherence to legal, regulatory, and company policies. They drive operational quality initiatives, oversee quality management systems, and ensure accurate data reporting for clinical trials.
Provide pre-sales and post-sales technical support, including product demonstrations, hands-on training, and troubleshooting for customers. Collaborate with sales and cross-functional teams to build long-term customer relationships and support business objectives.
The Buyer III manages day-to-day procurement activities, supplier relationships, and material requirements to ensure efficient manufacturing operations. They are responsible for identifying supply chain issues, driving cost reduction initiatives, and collaborating with cross-functional teams to resolve escalations.
The Associate Project Manager supports the Project Lead by managing project-specific activities, including project plans, reports, and vendor coordination. They are also responsible for overseeing project finances, risk registers, and ensuring compliance with regulatory and organizational standards.
Develop and execute strategic territory plans to drive revenue growth and identify new business opportunities within the diagnostic market. Build and maintain strong relationships with healthcare professionals while providing consultative solutions that address clinical and operational needs.
The Safety Administrator coordinates the review of adverse events, protocol inquiries, and data for clinical trials while managing project documentation and committee logistics. They act as a liaison between internal teams, clients, and external vendors to ensure project timelines and safety standards are met.
The Clinical Trial Manager is responsible for achieving clinical deliverables within contractual time, quality, and cost expectations. They manage clinical operational aspects, lead study teams, and ensure compliance with ICH GCP and regulatory standards.
The Senior Safety Specialist performs day-to-day pharmacovigilance activities, including the collection, monitoring, and assessment of safety information. They also provide leadership, mentor junior staff, and ensure compliance with global regulatory requirements.
The Global Study Lead is responsible for the end-to-end operational management of global clinical studies, ensuring alignment between global strategy and regional execution. They lead cross-functional teams, manage CRO vendors, oversee study budgets, and ensure compliance with regulatory standards and quality requirements.
Develop and manage strategic customer relationships across a diverse portfolio of scientific products to drive revenue growth. Collaborate with technical specialists and product managers to deliver comprehensive solutions that meet complex customer research and manufacturing needs.
The Local Clinical Trial Manager is accountable for the end-to-end delivery of clinical studies within the country, ensuring they meet time, budget, and quality expectations. They lead local study teams, manage site selection, oversee regulatory submissions, and ensure compliance with GCP and local guidelines.
The Biostatistician will serve as a lead statistician for clinical research projects, overseeing statistical analyses, protocol design, and the development of analysis plans. They will also coordinate with data management and programming teams while ensuring compliance with departmental SOPs and project timelines.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. They ensure site preparedness, manage essential documentation, and assist with study-specific systems and vendor coordination.
You will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. This involves conducting on-site or remote visits, managing documentation, and resolving site-level issues to maintain audit readiness.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage customer expectations, and ensure compliance with regulatory requirements and internal SOPs.
Develop and manage relationships with academic and industry customers to achieve sales objectives for the Olink proteomics portfolio. Drive territory growth by identifying customer needs, providing technical solutions, and managing biomarker discovery projects.
Lead and execute global CMC regulatory strategies for biological products while ensuring compliance with US and Canadian regulatory requirements. Manage the preparation, review, and submission of regulatory dossiers and oversee post-approval lifecycle management activities.
The Site Contract Specialist manages the drafting, negotiation, and finalization of investigator contracts and budgets while ensuring compliance with company and client standards. They also coordinate with internal teams to align site startup activities with project timelines and provide mentorship to junior staff.
Provides administrative and technical support to clinical research project teams, including coordinating project documents, records, regulatory materials, communications, and local payments. Supports reporting and data collection, resolves documentation findings, coordinates meetings and minutes, and assists with project management activities and study dashboards.
Provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. Manages safety variables, performs medical reviews of adverse events, and provides consultation to project teams and clients.
The representative will achieve territory revenue goals by proactively developing a sales pipeline and managing customer relationships. They will also collaborate with channel partners to promote the company's broad product portfolio and maximize business results.
The Country Approval Specialist coordinates local regulatory submissions and provides strategic advice to ensure clinical trial site activation. They manage documentation, maintain tracking databases, and collaborate with internal departments to meet project timelines.
The Senior Patient Recruitment and Engagement Lead will provide strategic leadership for global patient recruitment and retention across clinical trials. This role involves managing recruitment campaigns, overseeing vendor performance, and collaborating with cross-functional teams to ensure enrollment success and quality data collection.
The Senior Account Manager will drive revenue growth by promoting a comprehensive portfolio of analytical instruments and consumables to various scientific accounts. This field-based role involves developing strategic relationships with key decision-makers and coordinating cross-functional resources to provide exceptional customer experiences.
The Account Manager is responsible for selling and supporting Chromatography and Mass Spectrometry products while maintaining long-lasting customer relationships. They identify new client opportunities, negotiate contracts, and lead sales strategies to meet quarterly objectives within their assigned territory.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global submission strategies. They also provide regulatory advice to internal clients and ensure site start-up activities are aligned with project timelines.
The Import/Export Coordinator manages the compliant movement of clinical supplies by coordinating with logistics providers, customs brokers, and internal teams. They are responsible for preparing shipping documentation, monitoring international shipments, and resolving any logistics or customs-related issues.
Provide scientific and technical application support for flow cytometry technologies to customers across the Southern California territory. Collaborate with sales and product teams to optimize experimental workflows, troubleshoot complex issues, and drive product adoption.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial site agreements and investigator grant budgets. They ensure compliance with internal processes and client expectations while managing risks and coordinating with internal teams to meet site activation timelines.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects in terms of quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
The Senior Site Contract Specialist manages the preparation, negotiation, and finalization of investigator contracts while ensuring compliance with legal and financial parameters. They also coordinate with internal teams to align site startup activities and provide mentorship to junior staff.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage essential trial documentation.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and adherence to ICH-GCP guidelines. They manage site documentation, facilitate communication between stakeholders, and perform risk-based monitoring activities to ensure trial integrity.
The Clinical Research Associate I coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage essential trial documentation.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They manage site documentation, facilitate communication between stakeholders, and ensure trial materials are properly handled and reported.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including site preparedness and remote monitoring activities. They are responsible for document collection, system access management, and reconciliation of study data in accordance with SOPs and regulatory guidelines.
The Operational Bidding Specialist evaluates RFPs and collaborates with cross-functional teams to develop accurate, customer-focused proposal budgets. They are responsible for maintaining corporate databases, tracking reports, and ensuring proposal assumptions align with study specifications.
You will develop and validate analytical applications while serving as a subject matter expert to support customer research and innovation. The role involves collaborating with R&D and commercial teams to translate customer needs into optimized scientific workflows.
You will drive market adoption of NGS library prep solutions by acting as a technical authority and consultative partner for research and clinical customers. Additionally, you will manage complex sales cycles and collaborate with internal teams to ensure seamless customer onboarding and revenue growth.
The Senior BioProduction Account Manager will own overall revenue, bookings, and account performance across all Thermo Fisher BioProduction business units within assigned customer sites. They will lead customer relationships, develop accurate forecasts, and coordinate integrated workflow solutions by collaborating with technical and product management teams.
The Senior Programmer Analyst leads bioinformatics programming activities for clinical research projects and manages data across multiple systems. They are also responsible for mentoring junior team members and contributing to departmental infrastructure and SOP development.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They will provide exceptional customer service while supporting customers across research, industrial, and healthcare settings.
The Medical Director provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. They also provide medical consultation to project teams, monitor safety variables, and review serious adverse events.
The Clinical Program Quality Excellence Lead manages cross-functional teams to ensure GCP inspection readiness and high-quality deliverables throughout the clinical study lifecycle. They provide guidance on operational processes, oversee TMF performance, and facilitate audit and inspection preparation.
Lead global labeling strategy and author key regulatory documents such as the Target Product Label and Company Core Data Sheet. Act as a subject matter expert and liaison between internal teams, external clients, and health authorities to ensure regulatory compliance and high-quality submissions.
The 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 Customer Success Manager is responsible for selling service products, such as maintenance contracts and warranty extensions, to existing and new customers. They will manage contract renewals, build long-term client relationships, and utilize CRM systems to track sales activities and achieve financial targets.
The role involves coordinating clinical monitoring and site management processes to ensure trial compliance with protocols, ICH GCP guidelines, and regulatory standards. Responsibilities include conducting risk-based monitoring, verifying data accuracy, and maintaining collaborative relationships with investigator sites.
The Site Contract Specialist drafts, negotiates, and executes clinical study site contracts and investigator grant budgets. They also maintain professional relationships with sites and ensure all finalized documents are accurately processed and uploaded to the eTMF system.
The Global Study Lead is responsible for the end-to-end management of global clinical studies, ensuring alignment between global strategy and regional execution. They lead cross-functional teams, manage CRO vendors, and oversee study budgets, timelines, and regulatory compliance.
Develop and implement strategic sales plans to drive the adoption of diagnostic testing within the assigned territory. Manage key account relationships and provide consultative solutions to healthcare professionals to meet sales targets.
Develop and implement strategic sales plans to drive the adoption of diagnostic testing and manage key account relationships. Collaborate with cross-functional teams to provide tailored solutions while ensuring customer satisfaction and achieving sales targets.
The Senior Manager will lead a portfolio of applied AI initiatives, overseeing technical design, development, and production deployment across generative and agentic AI. They will also coach multidisciplinary teams and drive the creation of reusable enterprise AI capabilities to ensure scalable and reliable business solutions.
The Project Manager serves as the primary lead for non-interventional clinical trials, ensuring the project is delivered on time, within budget, and to high quality standards. They are responsible for managing cross-functional teams, maintaining sponsor relationships, and ensuring compliance with regulatory requirements and internal SOPs.
The Medical Director provides medical oversight for clinical trials to ensure compliance with regulatory requirements, SOPs, and good clinical practice. They also provide medical consultation to project teams, review safety data, and support business development activities.
Conduct and manage internal and external clinical audits, identify quality and compliance issues, determine root causes, and develop corrective strategies. Report audit findings, lead quality improvement initiatives, develop compliance tracking tools, and mentor staff while supporting clinical development programs.
The Expanded Access Manager will lead the operational support for post-trial managed access programs, including budget coordination and vendor management. They will collaborate with cross-functional teams to ensure regulatory compliance and continuity of access for patients.
The Global Study Manager is accountable for the end-to-end operational delivery of clinical studies, ensuring they meet time, quality, and budget targets. They lead matrix teams, manage vendors, and oversee risk mitigation strategies throughout the study lifecycle.
The Technical Sales Specialist will support field sales activities and customer engagement across the downstream bioproduction workflow portfolio in Germany, the Netherlands, and V4 countries. They will collaborate with account managers and cross-functional teams to identify customer needs, provide technical expertise, and position Thermo Fisher Scientific's solutions.
The Import Export Coordinator executes import and export activities in compliance with company and client requirements. They also maintain documentation files and participate in department project teams to ensure regulatory standards are met.
The Field Application Scientist provides technical training, application support, and pre-sales consultation for HID products across Western North America. They collaborate with internal teams and customers to ensure successful implementation and optimization of forensic workflows.
Manage end-to-end recruitment across multiple business functions while serving as a trusted advisor to hiring managers. Proactively source talent, build pipelines, and utilize recruiting metrics to drive effective hiring strategies.
The Technical Project Lead is responsible for owning the technical delivery of laboratory informatics solutions, including design, architecture, and implementation. They act as a primary technical point of contact for customers and collaborate with internal teams to ensure projects are delivered on time and within budget.
You will identify and pursue new business opportunities while developing strategic relationships with key accounts to drive growth. Additionally, you will collaborate across divisions to deliver comprehensive solutions and manage the sales pipeline through the CRM system.
The Clinical Trial Coordinator provides administrative and technical support to project teams while overseeing trial activities and documentation. They act as a cross-functional liaison, manage study-specific systems, and ensure compliance with regulatory standards and project timelines.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate process improvements across clinical trials.
The Global Clinical Integration Lead will provide strategic project and programme management support for complex business development, integration, and transition activities within Clinical Operations. They will coordinate cross-functional stakeholders, develop clear roadmaps, and ensure that high-priority initiatives are effectively planned and executed.
The Digital Account Manager will drive revenue growth and customer retention across a large portfolio of accounts in the Nordics using a digital-first approach. They will manage a sales pipeline, engage customers through various digital channels, and collaborate with cross-functional teams to optimize the online customer journey.
The Field Service Engineer is responsible for the installation, maintenance, and qualification of standardized scientific systems within the Freiburg region. They will perform routine repairs, document service activities, and provide technical support to customers while escalating complex issues to the appropriate teams.
The recruiter will manage the full recruitment lifecycle for high-volume positions, including sourcing, candidate engagement, and onboarding. They will collaborate with hiring managers and HR colleagues to build candidate networks while ensuring compliance with employment laws.
Design, develop, and deliver technical sales learning programs to enhance commercial capability and sales productivity across the Asia Pacific, Japan, and Greater China regions. Collaborate with cross-functional teams to translate complex scientific concepts into engaging learning experiences while managing digital content and reporting on training metrics.
You will lead a sales team to drive customer success and business growth while executing strategic sales plans across research and clinical markets. Additionally, you will maintain strong customer relationships, analyze market trends, and ensure the team meets or exceeds sales and profitability targets.
You will be responsible for the configuration, implementation, and deployment of Thermo Scientific SampleManager LIMS solutions across various laboratory environments. This involves translating functional requirements into technical workflows, managing system integrations, and supporting data migration and validation activities.
You will serve as a technical expert in downstream bioproduction, providing comprehensive support, training, and troubleshooting for customers. Additionally, you will collaborate with internal R&D teams to provide feedback and contribute to product development and strategic projects.
The Director of Product Specialists will lead product strategy and oversee the performance of product specialist teams. This role involves driving business results through effective team management and cross-functional collaboration.
The manager will oversee product support operations and ensure high-quality service delivery for the company's product lines. They are responsible for leading the support team and coordinating with internal departments to resolve complex customer issues.
The Customer Service Representative will handle customer inquiries and provide support in a professional manner. They are responsible for maintaining accurate records and ensuring high levels of customer satisfaction.
Drive sales growth and manage key accounts across academic, government, and industrial sectors within the assigned territory. Execute strategic sales initiatives, maintain a healthy sales pipeline, and build strong relationships with key stakeholders to achieve revenue targets.
The role involves performing standard customer service representative duties. The position operates on a standard Monday through Friday schedule.
The manager will oversee product support operations to ensure high-quality service delivery. They are responsible for managing team performance and maintaining standard office workflows.
The Medical Director provides medical oversight for clinical trials, ensuring adherence to regulatory requirements and company SOPs. They also manage safety profiles, perform medical reviews of adverse events, and provide consultation to investigators and project teams.
Provide technical support including installation, preventative maintenance, and repair of laboratory equipment while managing customer relationships. Lead commissioning and qualification protocols and ensure timely service delivery and performance metrics are met.
The Associate Director/Director will lead global regulatory strategy and execution for late-stage development programs through marketing authorization. They will coordinate cross-functional submissions, manage health authority interactions, and ensure compliance across the product lifecycle.
Oversee end-to-end clinical study delivery, including study plans, vendors and CROs, country progress, budgets, supplies, risks, and cross-functional team communications. Maintain inspection readiness through oversight of study data and eTMF completeness, while resolving or escalating delivery issues and mentoring colleagues.
The Country Approval Specialist manages and coordinates local regulatory submissions and site start-up activities in alignment with global strategies. They provide regulatory advice, negotiate site budgets, and ensure all trial documentation is maintained according to SOPs.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities to ensure site activation timelines and compliance standards are met.
The Senior Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They also act as a study lead, facilitate cross-functional liaison, and support process improvement initiatives.
The Country Approval Specialist manages and coordinates local regulatory submissions and provides strategic regulatory advice to internal clients. They also ensure site start-up activities align with submission timelines and maintain accurate trial status documentation.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global strategies. They also provide regulatory advice to internal clients and ensure site start-up activities meet project timelines.
Manage all clinical operational and quality aspects of allocated studies of moderate to high complexity in compliance with ICH GCP. Ensure clinical deliverables meet customer time, quality, and cost expectations while maintaining project profitability.
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. This role involves leading clinical teams, developing monitoring plans, and maintaining compliance with ICH GCP and regulatory standards.
The Pharmacovigilance Coordinator manages safety documentation, tracks adverse events, and coordinates project meetings for global clinical trials. They also interface with internal and external stakeholders to ensure audit readiness and compliance with regulatory standards.
The Account Manager is responsible for selling and supporting chromatography and mass spectrometry products while maintaining long-term customer relationships. They will identify new client opportunities, negotiate contracts, and lead sales strategies to meet quarterly objectives within their assigned territory.
The Principal Site Contract Specialist leads the negotiation and finalization of complex site contracts while ensuring compliance with budgetary and legal parameters. The role also involves mentoring junior staff, developing training plans, and coordinating with internal departments to ensure efficient site activation.
The Account Manager II will support revenue growth by developing and maintaining strategic customer relationships while promoting a portfolio of scientific products. They will implement sales strategies, identify new business opportunities, and provide excellent support to help customers achieve their goals.
The Site Contract Specialist will draft, review, and negotiate clinical trial agreements and investigator grant budgets with study sites. They will also coordinate with internal functional teams to ensure site activation timelines are met while managing legal and financial risks.
The Senior Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions in alignment with global strategies. They serve as a primary contact for investigators and regulatory authorities to ensure timely site activation and compliance.
The Business Development Associate will act as the initial touchpoint for new customers to identify and qualify business opportunities within the pharmaceutical industry. They will support outbound campaigns, manage CDA/NDA execution, and coordinate client meetings to build a strong pipeline of prospects.
The Field Applications Scientist provides technical support, training, and product demonstrations to customers to optimize their scientific workflows. They collaborate with cross-functional teams including sales and R&D to drive business growth and ensure customer success.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of projects regarding quality, time, and cost. They lead cross-functional teams to meet deliverables while ensuring compliance with regulatory requirements and internal SOPs.
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, oversee project financials, and ensure compliance with ICH GCP and regulatory standards throughout the study lifecycle.
The Site Account Representative will manage on-site asset management and laboratory support services for key customer accounts. They will serve as the primary point of contact to ensure seamless service delivery and high customer satisfaction.
The Sales Development Associate qualifies inbound leads and engages prospective customers to identify new business opportunities. They support field sales teams by managing lead information in CRM systems and tracking biotech funding to drive account development.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Conducts on-site and remote visits to assess regulatory adherence and manages essential trial documentation.
The Technical Sales Specialist is responsible for driving revenue growth for mass spectrometry and chromatography products by identifying new opportunities and supporting account managers. They act as a technical advisor to customers, managing the sales process from initial prospecting through to deal closure.
The Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety variables, perform medical reviews of adverse events, and provide medical consultation to project teams and clients.
The role involves providing statistical leadership for clinical trials, including study design, analysis, and reporting. You will collaborate with cross-functional teams and act as a project lead to ensure scientific rigor and regulatory compliance.
The Procurement Assistant is responsible for managing purchase requisitions, purchase orders, and vendor invoices within the Global Clinical Supplies Team. They also ensure financial tracking accuracy and resolve procurement-related discrepancies in collaboration with cross-functional teams.
Develop and execute strategic territory account plans to drive growth across allergy and autoimmunity portfolios while managing the full sales cycle. Build trusted relationships with key decision-makers in healthcare and laboratories to improve patient pathways and achieve sales targets.
The Account Development Analyst supports RFP funnel growth by researching prospective clients, identifying leads, and nurturing relationships. They also manage marketing-generated leads, provide team training, and develop strategic plans to support sales volume.
The Medical Project Coordinator will support drug safety operations by reviewing safety data, identifying trends, and ensuring compliance with regulatory standards. They will also manage project implementation, coordinate with stakeholders, and resolve complex safety-related issues.
The Senior Clinical Team Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, monitor study performance, and ensure compliance with ICH GCP and regulatory standards.
The Sales Specialist will drive growth for the Olink Proteomics portfolio by identifying new business opportunities and managing relationships across academia, biotech, and pharma sectors. The role requires significant field time to engage with researchers and key opinion leaders to align proteomics solutions with their scientific research needs.
The Import/Export Coordinator is responsible for planning and executing complex import and export activities for clinical studies. They ensure all logistics are compliant with PPD, client requirements, and global regulations while maintaining accurate metrics and documentation.
The Clinical Research Associate will perform and coordinate all aspects of the clinical monitoring process while working within multi-national project teams. They are responsible for ensuring high levels of customer service and maintaining quality and accuracy across multiple clinical research projects.
The role involves performing and coordinating clinical monitoring and site management processes to ensure protocol and regulatory compliance. Responsibilities include conducting remote or on-site visits, managing documentation, and ensuring data reliability through risk-based monitoring.
The Start-up Team Manager oversees site activation activities, ensuring compliance with regulatory standards and project timelines across assigned regions. They facilitate collaboration between internal teams and trial sites while managing technical, operational, and risk-mitigation aspects of clinical studies.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence and manage documentation throughout the clinical trial lifecycle.
The FSP Manager Clinical Operations oversees, trains, and mentors a team of clinical staff while ensuring adherence to SOPs and project metrics. They also collaborate with leadership on resourcing, process improvement, and strategic business development initiatives.
The Clinical Sales Specialist will drive revenue growth and develop new business opportunities within hospitals and laboratories across the assigned territory. They will serve as a trusted advisor by applying a consultative approach to understand customer needs and provide tailored diagnostic solutions.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of cross-functional projects in terms of quality, time, and cost. They are responsible for driving risk identification, issue resolution, and ensuring team compliance with organizational policies and regulatory requirements.
The Associate Manager Clinical Operations oversees daily line management, coaching, and professional development for clinical operations staff. They collaborate with senior management on strategic planning, resource allocation, and ensuring adherence to company SOPs and quality standards.
The Business Development Associate will review, qualify, and prioritize inbound leads while supporting field sales teams with prospecting and account development. They will also maintain accurate data in CRM systems and track biotech funding events to identify new sales opportunities.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage clinical trial documentation, perform file reviews, and coordinate with internal and external stakeholders to meet project timelines.
The Clinical Trial Coordinator provides administrative and technical support to project teams while facilitating project activities across global clinical trials. They are responsible for maintaining study documentation, ensuring compliance with regulatory standards, and managing project-specific trackers and systems.
The Market Development Specialist identifies and develops commercial growth opportunities for Precision Diagnostics solutions by engaging healthcare providers and partners. They manage a defined book of business, monitor adoption data, and collaborate across internal teams to drive sustained utilization and market expansion.
The Demand and Supply Manager will design and implement inventory management plans to forecast supply for global clinical trials using sound supply chain techniques. They will also partner with cross-functional teams to optimize supply strategies and ensure continuity of subject supply while managing financial forecasts.
You will perform and coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Additionally, you will manage site relationships, conduct risk-based monitoring, and mentor junior team members to ensure data reliability and audit readiness.
The Regulatory Affairs Manager will own regulatory decision-making for clinical programs and drive cross-functional teams to execute regulatory strategies. They are responsible for ensuring compliance, managing project budgets, and maintaining effective client interfaces throughout the product development lifecycle.
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They are responsible for site initiation, ongoing monitoring, issue resolution, and trial close-out activities while maintaining effective communication with investigative sites.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include verifying document collection, managing site supplies, and assisting with study-specific systems and vendor coordination.
Provides administrative and technical support to the project team, including site activation activities and audit readiness. Manages clinical trial documentation, ensures system databases are current, and coordinates with internal departments to meet project deadlines.
Performs and coordinates all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data accuracy, manage documentation, and maintain collaborative relationships with investigational sites.
The Operational Bidding Specialist prepares and delivers competitive, high-quality operational bids and proposals for regulatory and medical writing services. They collaborate with internal teams to define bid strategies, labor requirements, and budget assumptions while ensuring alignment with client specifications.
The Senior Safety Reporting Specialist will lead the preparation and submission of complex safety reports while ensuring compliance with international pharmacovigilance regulations. They will also manage large-scale projects, provide guidance to team members, and contribute to the development of departmental procedural documents.
The Country Approval Specialist prepares, reviews, and coordinates local regulatory submissions while providing strategic advice to internal clients. They also manage site start-up activities and ensure all submission processes align with global strategic goals and timelines.
The Clinical Data Team Lead acts as the primary data manager for clinical studies, overseeing data management activities and ensuring operational excellence. They serve as a liaison between the project team and clients while mentoring junior staff and managing project documentation.
The Operations Strategy Consultant manages the proposal development process to increase RFP hit rates and business growth. They are responsible for defining operational strategies, overseeing budgets, and collaborating with cross-functional teams to ensure successful clinical trial project delivery.
The Clinical Trial Coordinator provides administrative and technical support to project teams while ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between internal teams and clinical sites.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess site performance, manage documentation, and resolve issues to maintain audit readiness.
The Biostatistician II acts as a lead statistician, independently managing analysis database creation, statistical programming, and the development of analysis plans. They also provide mentorship to junior team members and coordinate directly with sponsors and project teams to ensure adherence to statistical methodology and project timelines.
The Account Manager will drive revenue growth by developing strategic customer relationships and promoting a portfolio of scientific products. They are responsible for implementing sales strategies, identifying new business opportunities, and providing expert support to customers.
You will drive revenue growth by developing and maintaining strategic customer relationships while promoting a portfolio of scientific products. Additionally, you will implement sales strategies, identify new business opportunities, and provide support to help customers achieve their scientific goals.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence using a risk-based approach. They will manage site processes, facilitate communication between stakeholders, and ensure trial documentation is complete and audit-ready.
You will develop and implement strategic sales plans while managing key account relationships to drive revenue growth. Additionally, you will serve as a trusted advisor to customers, providing tailored scientific solutions through both virtual engagement and site visits.
The Field Service Engineer II is responsible for installing, maintaining, troubleshooting, and repairing complex analytical and scientific instruments. They will provide exceptional customer service and support while ensuring all work adheres to safety and quality standards.
You will drive revenue growth by promoting a portfolio of analytical instruments and consumables to key decision-makers. This role involves managing complex sales cycles and building strategic relationships across government, academic, clinical, and industrial sectors.
The Strategic Account Manager is responsible for driving reagent revenue growth and customer retention across a portfolio of laboratory accounts. They will develop strategic account plans and serve as the primary point of contact for stakeholders in hospitals, reference labs, and integrated health systems.
Perform on-site installation, preventive maintenance, and repairs of electron microscopy systems while providing technical support to customers. Coordinate work schedules and ensure high levels of customer satisfaction through effective communication and reporting.
The QA Auditor II will conduct and lead various client, internal, and GCP audits while ensuring regulatory compliance and quality standards. They will also provide GCP consultation to project teams and prepare audit findings for internal and client meetings.
The Pharmacovigilance Physician provides medical oversight for pharmacovigilance activities, ensuring compliance with regulatory requirements and company SOPs. They perform medical review and analysis of serious adverse events, signal detection, and contribute to the management of product benefit-risk profiles.
The 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.
You will coordinate all aspects of clinical monitoring and site management to ensure trials are conducted according to protocols and regulatory standards. This includes performing remote or on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The Business Development Associate is responsible for qualifying inbound leads, engaging prospective customers, and routing opportunities to field sales representatives. They also support sales teams with prospecting, account development, and maintaining accurate data within the CRM system.
The Sales Development Representative II will identify and develop new business opportunities while nurturing customer relationships across a scientific portfolio. They will collaborate with cross-functional teams to provide innovative solutions that help customers advance their research and healthcare outcomes.
The Field Service Engineer is responsible for the installation, maintenance, troubleshooting, and repair of sophisticated analytical and scientific instruments. They will provide exceptional customer service while supporting research, industrial, and healthcare clients.
The Regulatory Affairs Specialist is responsible for reviewing and approving country- and site-level essential documents to ensure compliance and support timely site activation. They also maintain knowledge of regulatory guidelines and track review details within the company's data tracking systems.
The Field Service Engineer will provide installation, maintenance, troubleshooting, and repair services for Phadia ImmunoDiagnostics systems at customer sites. They will manage their own field-based workload while collaborating with technical support, sales, and other colleagues to ensure optimal instrument performance.
Provide post-sales technical support through training, troubleshooting, and workflow optimization for pharmaceutical analytics solutions. Collaborate with customers to implement solutions while acting as a customer advocate to influence product improvements and support sales activities.
The Senior Clinical Trial Manager is responsible for managing all clinical and start-up activities, ensuring projects meet quality, time, and cost expectations. They act as the primary point of contact for sponsors and coordinate cross-functional teams to drive operational excellence in clinical trials.
The Compliance Manager will lead and manage GxP audits and regulatory inspections for clinical trials across the APAC region. They will provide consultation on inspection readiness, facilitate audit hosting, and support project teams in developing CAPAs to address non-conformances.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage documentation, and facilitate communication between investigative sites and project teams.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They conduct on-site or remote visits to assess regulatory adherence and manage essential trial documentation.
The Medical Writer is responsible for planning, coordinating, and authoring high-quality clinical and scientific documents such as study reports and protocols. They also collaborate with internal and external clients to ensure operational excellence and compliance with quality standards.
The Clinical Research Associate coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site and remote visits to assess regulatory adherence, manage documentation, and resolve site-related issues.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include maintaining essential documents, coordinating site supplies, and assisting with study-specific system updates and data reconciliation.
Lead and develop a team of Clinical Sales Specialists to drive allergy testing growth and optimize lab utilization across the assigned district. Develop and execute strategic sales plans while cultivating advocacy and maintaining strong relationships with key healthcare decision-makers.
The Field Service Engineer is responsible for the installation, maintenance, troubleshooting, and repair of laboratory instruments within an assigned territory. They must build strong customer relationships while ensuring service objectives and documentation requirements are met.
The Field Service Engineer will assemble, install, calibrate, and maintain electromechanical instrumentation while ensuring high-quality service and customer satisfaction. The role involves conducting root cause analysis, performing preventative maintenance, and managing administrative service records.
Lead client programs within the regulatory medical writing team by managing project timelines, budgets, and client relationships. Ensure operational excellence and high-quality document delivery while serving as a subject matter expert and mentor to junior staff.
The Technical Sales Specialist will develop and execute business strategies for the Cell Culture and Cell Therapy portfolio across the Nordic region. They will drive new business opportunities, manage customer relationships, and collaborate with internal teams to provide technical solutions for bioprocessing workflows.
The Safety Writer III is responsible for planning, coordinating, and delivering safety writing services for clinical trials and marketed products within a regulated pharmacovigilance environment. This role involves leading project teams, conducting data reviews, and ensuring all deliverables comply with regulatory standards and internal policies.
The Clinical Trial Manager is responsible for managing clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, maintain study documentation, and ensure compliance with ICH GCP and regulatory requirements.
The Senior Clinical Research Associate ensures clinical studies are conducted in compliance with protocols, ICH GCP, and regulatory requirements. They perform and coordinate all aspects of the clinical monitoring process to ensure data accuracy and subject safety.
Manage clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulatory standards. Perform site monitoring activities, maintain inspection readiness, and collaborate with project teams to deliver high-quality clinical trials.
The Business Development Executive is responsible for driving profitable growth by securing new molecules and expanding services within assigned biotech accounts. They will execute territory sales plans, manage the sales cycle from outreach to contract execution, and collaborate cross-functionally to deliver integrated solutions.
The Clinical Research Associate I monitors investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They facilitate communication between sites and project teams while managing essential documentation and trial status reporting.
You will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. This includes conducting on-site or remote visits, performing root cause analysis, and managing corrective actions to maintain audit readiness.
Manage and coordinate clinical monitoring and site management activities to ensure trials comply with protocols, ICH-GCP, and regulatory standards. Perform remote and on-site monitoring, including source data verification and site deficiency resolution, to maintain data quality and patient safety.
The Senior Clinical Research Associate performs and coordinates clinical monitoring and site management processes to ensure protocol and regulatory compliance. They conduct remote or on-site visits to assess data accuracy, manage site documentation, and facilitate effective communication between investigative sites and the project team.
The Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management to ensure protocol compliance and data reliability. They conduct on-site or remote visits, manage documentation, and facilitate communication between investigative sites and the project team.
The Senior Medical Director will provide medical monitoring and safety evaluation for clinical trials within the pharmacovigilance department. They will also lead medical aspects of contracted tasks and support business development activities by presenting safety processes to clients.
The Senior Account Manager will drive profitable growth by developing strategic customer relationships and managing the full sales cycle for materials and surface analysis solutions. They will collaborate with technical and service teams to identify customer needs, respond to tenders, and provide effective product and workflow recommendations.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data reliability through rigorous review and problem-solving.
The Project Budget Coordinator will manage clinical trial budgets, track indirect costs, and provide financial reporting for project teams. They will also coordinate cross-functional activities and handle purchase requisitions within the clinical supplies lifecycle.
The Field Service Engineer will install, maintain, troubleshoot, and repair complex analytical instruments such as SEM and SDB systems. They are responsible for providing exceptional customer service and training while documenting all service activities.
Lead and mentor a team of application scientists to provide high-quality technical support and consultative services for proteomics workflows. Collaborate with sales teams to drive market presence while ensuring customer satisfaction through effective demonstrations and troubleshooting.
The Senior Sales Manager will lead and develop commercial teams to drive strategic growth and achieve revenue targets within the Southeast region. They are responsible for implementing sales strategies, managing pipelines, and fostering strong customer relationships across the life sciences portfolio.
You will represent a portfolio of scientific instruments and solutions to drive revenue growth and customer success. As a technical advisor, you will collaborate with cross-functional teams to implement sales strategies and provide expertise throughout the sales cycle.
The Senior Account Manager will manage key client relationships, drive revenue growth, and oversee project execution while ensuring high customer satisfaction. Additionally, the role involves providing leadership, coaching, and talent development to a team of account managers to support business objectives.
Provide onsite service including repairs, preventive maintenance, and installation of IDD analyzers at customer sites. Collaborate with internal partners and provide technical training to Biomedical Engineering Technicians and operators.
Provides medical oversight for clinical trials, ensuring adherence to regulatory requirements, SOPs, and good clinical practices. Manages safety variables, performs medical reviews of adverse events, and provides medical consultation to project teams and investigators.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform on-site and remote monitoring activities, manage documentation, and resolve site-related issues to ensure data reliability and subject safety.
The role involves coordinating all aspects of clinical monitoring and site management to ensure trials are conducted according to protocols and ICH-GCP guidelines. You will perform risk-based monitoring, ensure data accuracy, and maintain collaborative relationships with investigational sites.
You will coordinate all aspects of the clinical monitoring and site management process to ensure trial compliance with protocols and regulatory standards. This includes conducting remote or on-site visits, managing documentation, and ensuring data accuracy through rigorous review processes.
The Associate Director leads the innovation landscape by translating strategic priorities into validated discovery themes and actionable opportunities. They oversee a portfolio of projects, ensuring rigorous evidence-based decision-making and cross-functional alignment across digital, data, and scientific teams.
The Innovation Director drives innovation across the organization by shaping and overseeing a portfolio of high-impact opportunities aligned with strategic business priorities. They act as a senior interface between innovation teams and execution teams to ensure strategic intent is maintained throughout the validation and transition processes.
The Director provides enterprise-level leadership across multiple strategic FSP accounts, driving portfolio strategy, operational transformation, and client partnership growth. They act as a strategic advisor to internal and external leadership to influence long-term delivery models and organizational performance.
The Clinical Specialist will support business growth through technical sales expertise, customer relationship management, and strategic sales initiatives. They are responsible for conducting product demonstrations, providing application support, and managing contract implementations to advance laboratory research.
You will coordinate all aspects of clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. This includes conducting on-site or remote visits, managing documentation, and performing data verification to ensure subject safety and data reliability.
The Global Study Manager will lead the operational strategy and end-to-end delivery of complex global clinical studies, ensuring adherence to timelines, budget, and quality standards. They will provide strategic leadership to cross-functional teams and act as the primary escalation point for operational issues.
The Senior Account Manager will drive revenue growth by managing strategic customer relationships and providing consultative sales for scientific products. They will collaborate with technical and support teams to deliver integrated automation solutions that advance critical research and manufacturing initiatives.
Provides nutrition expertise and operational support for clinical trial nutrition programs, including menu development and lifestyle intervention services. Collaborates with internal teams and stakeholders to ensure regulatory compliance and high-quality execution of study requirements.
Provides nutrition expertise and operational support for clinical trial nutrition programs, including menu development and lifestyle interventions. Collaborates with internal teams and stakeholders to ensure regulatory compliance and high-quality execution of study requirements.
The specialist will manage account profiling and develop relationships with key healthcare stakeholders to drive procalcitonin testing strategies. They are responsible for delivering clinical education programs and meeting annual operating growth targets within their designated region.
The Local Clinical Trial Manager leads the local study team and serves as the operational point-of-contact to ensure clinical deliverables meet time, budget, and quality expectations. They are responsible for managing study sites, regulatory submissions, vendor oversight, and ensuring compliance with GCP/ICH guidelines.
Drive clinical demand and adoption of Procalcitonin and other innovative biomarkers through engagement with healthcare professionals. Develop hospitals and healthcare institutions by building relationships and supporting the implementation of biomarker-guided clinical pathways.
The Clinical Sales Specialist will develop and implement strategic sales plans to drive growth within healthcare segments while managing key account relationships. They will provide consultative support to physicians and laboratory staff to ensure the effective adoption and utilization of diagnostic testing solutions.
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include maintaining study documentation, coordinating vendor data, and assisting with site preparedness and patient-facing materials.
The Account Manager will drive commercial growth by developing strategic territory plans and managing relationships with clinical laboratories and key decision-makers. They are responsible for the full sales cycle, from identifying new business opportunities to closing deals and ensuring long-term customer satisfaction.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage essential documentation in accordance with ICH-GCP guidelines.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within budget. They act as a cross-functional liaison, manage study documentation, and facilitate communication between internal teams and clinical sites.
Provide expert installation, maintenance, and repair services for sophisticated analytical and microscopy equipment. Build strong customer relationships while resolving complex technical issues and training users on system performance.
The Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety data, perform signal detection, and provide medical consultation to project teams and clients.
Perform on-site installation, maintenance, troubleshooting, and repair of complex IC-LC-MS analytical instruments. Actively promote service contracts and maintain strong customer relationships while ensuring compliance with safety and quality standards.
The Senior Manager will oversee clinical data management staff, including performance management, coaching, and resource allocation. They will also ensure operational quality and compliance with procedures while supporting study portfolios to meet client expectations.
The Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring visits and system updates.
The Senior Clinical Research Associate is responsible for the preparation, initiation, monitoring, and closure of assigned clinical study sites to ensure compliance with international guidelines and local regulations. They act as the primary contact for study sites, driving performance and ensuring data quality through regular monitoring visits and risk assessments.
The Field Application Scientist will serve as a technical expert to support customers in adopting single-use upstream bioprocessing technologies and optimizing workflows. They will lead pre- and post-sales technical activities, provide troubleshooting, and deliver training to ensure customer success and regulatory compliance.
You will perform and coordinate clinical monitoring and site management activities to ensure trials adhere to protocols, ICH-GCP, and regulatory standards. This involves conducting on-site and remote monitoring, performing data verification, and maintaining clear communication with investigational sites.
The Business Development Executive is responsible for driving growth within health systems and laboratories by advancing the adoption of diagnostic testing solutions. This role involves managing the transition from onboarding to revenue realization while orchestrating internal resources to meet sales targets.
The Senior Technical Sales Specialist will drive revenue growth and customer success by applying technical expertise to identify opportunities and build strong client relationships. They will provide technical leadership, conduct product demonstrations, and act as a trusted advisor to help customers achieve their research and development goals.
The Clinical Research Associate will coordinate clinical monitoring and site management processes to ensure protocol compliance and data reliability. They are responsible for conducting site visits, managing documentation, and facilitating communication between investigative sites and the project team.
The Clinical Data Team Lead acts as the primary data manager for clinical studies, overseeing data management activities and ensuring operational excellence. They serve as a liaison between departments and clients while mentoring junior staff and managing project documentation and metrics.
The Senior Site Contract Specialist manages the drafting, negotiation, and finalization of investigator agreements while ensuring compliance with budgetary and contractual parameters. They also coordinate with internal teams to align site startup activities and provide mentorship to junior staff.
The Global Cold Chain & HVAC Leader provides technical leadership and functional expertise to establish global engineering standards for temperature-controlled storage and HVAC systems. This role drives network capability, manages capital planning, and ensures compliance and business continuity across the CTD network.
The Assistant CRA provides logistical and administrative support for clinical trial site management, including site preparedness, remote monitoring, and document collection. They also assist with system updates, vendor coordination, and reconciliation tasks to ensure compliance with SOPs and regulatory guidelines.
The Manager Clinical Operations oversees, trains, and coaches a team while managing performance through metrics and key performance indicators. They also collaborate with leadership on resourcing, ensure adherence to regulatory standards, and support project deliverables.
Develop and execute strategic territory account plans to drive growth in allergy and autoimmunity portfolios while managing distributor performance in the Baltic region. Collaborate with internal stakeholders and key opinion leaders to influence patient pathways and increase diagnostic test volume.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They will also manage site processes, facilitate communication between stakeholders, and ensure audit readiness throughout the clinical trial lifecycle.
The Advanced Application Specialist will optimize bioprocess workflows and drive technology adoption by providing expert consultative support to customers. They will act as a technical advisor throughout the process development and manufacturing lifecycle while collaborating with internal teams to shape product strategy.
Lead and oversee complex clinical trial start-up activities across multiple EU countries while ensuring adherence to regulatory requirements and project timelines. Manage cross-functional stakeholders, site activation processes, and financial/contractual aspects to ensure successful study delivery.
The Associate Director will lead EU regulatory strategy and provide expert guidance throughout the product lifecycle, from preclinical stages to post-approval. They will act as a key liaison between internal teams and regulatory authorities to ensure high-quality, timely submissions and compliance.
The Director of Project Management will oversee complex, cross-functional strategic initiatives to drive business growth and operational efficiency. This role involves establishing project governance frameworks and leading teams to deliver results aligned with corporate objectives.
The specialist will proactively build and cultivate relationships with physicians, healthcare professionals, and community leaders to drive clinical trial recruitment. They will manage regional outreach activities, attend community events, and collaborate with internal teams to meet enrollment objectives.
Drive sales growth in the clinical trials division by developing and implementing strategies to generate business from new and existing biotech accounts. Manage the full sales cycle, including lead generation, contract negotiation, and maintaining strategic relationships with key opinion leaders and C-suite executives.
The Senior Account Manager will increase revenue by managing strategic customer relationships and serving as a trusted advisor for scientific products. They will collaborate with technical and support teams to deliver comprehensive solutions that advance critical research and manufacturing initiatives.
Manages complex translation project lifecycles, including planning, scheduling, and risk management. Facilitates communication between project teams and clients while ensuring financial and administrative processes are completed.
The 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 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 developer will contribute to data acquisition, modeling, and mapping projects while supporting global business functions with reporting and analytics deliverables. They are also responsible for maintaining technical documentation, automating repetitive tasks, and providing support for operational incidents.
The role involves developing and integrating AI and data solutions using Databricks, SAP, and cloud AI services. You will also design ETL pipelines, automate data workflows, and provide operational support for data systems.
The Site Contract Specialist is responsible for drafting, reviewing, and negotiating clinical trial agreements and investigator grant budgets with study sites. They ensure compliance with internal processes and client expectations while coordinating with functional teams to meet site activation timelines.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal SOPs.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical trial projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal SOPs.
The Field Service Supervisor will lead and support a team of field service engineers to ensure exceptional service delivery and operational excellence. This role involves coordinating service activities, managing team performance, and maintaining strong relationships with customers and internal stakeholders.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The Drug Safety Specialist performs daily pharmacovigilance activities including data entry, coding, and the assessment of adverse events. They also coordinate regulatory reporting, maintain safety databases, and collaborate with project teams and investigators.
The Safety Reporting Coordinator provides administrative support for pharmacovigilance, including the submission, tracking, and archiving of safety reports. They also assist with audit readiness, reconcile clinical trial data, and train staff on safety reporting processes.
The Assistant Clinical Research Associate provides logistical and administrative support for site preparedness, study start-up, and remote monitoring activities. They collaborate with clinical teams to ensure data accuracy, regulatory compliance, and efficient execution of clinical trial protocols.
The Account Manager II will develop and maintain strategic customer relationships while promoting a portfolio of scientific products and services. They are responsible for implementing sales strategies, identifying new business opportunities, and providing excellent support to help customers achieve their goals.
The specialist will build and cultivate relationships with physicians, healthcare professionals, and community leaders to drive clinical trial recruitment. They will travel regionally to conduct outreach, attend community events, and manage a network to support enrollment goals.
The Recruitment Strategy Manager will lead the development and execution of strategic participant recruitment campaigns to meet clinical study enrollment goals. They will serve as a subject matter expert, integrating data, marketing insights, and cross-functional collaboration to optimize recruitment performance and budget efficiency.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring trial activities are completed on time and within quality standards. They manage study documentation, track project metrics, and act as a liaison between cross-functional teams and clinical sites.
The Regulatory Program Manager will partner with Global Regulatory Leads to develop and execute comprehensive regulatory strategies across all stages of product development. This role involves facilitating cross-functional subteam meetings, managing complex timelines, and ensuring alignment on regulatory deliverables and milestones.
The Qualified Person for Pharmacovigilance acts as the EU/UK QPPV for selected clients, ensuring compliance with EU Directive 2001/83/EC and associated regulatory guidance. They also contribute to scientific safety services, manage budgets, and promote QPPV services to potential clients.
The Technical Sales Specialist is responsible for driving revenue growth for HPLC products by identifying new client opportunities and supporting account managers. They act as a technical advisor throughout the sales cycle, from prospecting to closing, while providing product expertise and training to internal teams.
The Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of clinical projects regarding quality, time, and cost. They lead cross-functional teams, manage vendor relationships, and ensure compliance with regulatory requirements and internal policies.
Conduct and lead various GCP, client, and internal audits to ensure regulatory compliance and quality standards. Serve as a knowledgeable resource for operational departments and provide GCP consultation to project teams.
The Clinical Research Associate II coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and facilitate communication between investigative sites and the project team.
You will coordinate all aspects of clinical monitoring and site management to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting remote or on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
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.
The Field Service Engineer II is responsible for the installation, maintenance, troubleshooting, and repair of sophisticated analytical instruments like SEM, TEM, and FIB systems. They must provide exceptional customer service, conduct on-site training, and travel to customer sites to resolve technical issues.
Perform on-site installation, maintenance, troubleshooting, and repair of complex IC-LC-MS analytical instruments. Ensure high customer satisfaction while managing spare parts inventory and promoting service contracts.
The Clinical Trial Coordinator provides administrative and technical support to project teams, ensuring audit readiness and efficient site activation. They manage study documentation, reconcile metrics, and facilitate communication between internal teams and clinical sites.
The Field Application Scientist provides onsite technical support for purification products, assisting customers with process development, optimization, and troubleshooting. They also collaborate with sales and technical teams to drive product adoption and gather market feedback.
The Recruitment Specialist will manage full-cycle recruitment for diverse roles while serving as a strategic talent advisor to hiring managers. They will develop effective sourcing strategies, build talent pipelines, and ensure a positive candidate experience across business units.
The specialist will drive revenue growth by managing technical sales for ion chromatography products and acting as a trusted advisor to key accounts. They will collaborate with cross-functional teams to implement sales strategies, support new product introductions, and provide technical expertise throughout the sales cycle.
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.
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 Proposal Specialist creates and reviews compelling proposals and responses to client requests for information (RFIs) to position the organization as the optimal choice. They also liaise with subject matter experts to gather content and maintain strategic library resources for future use.
The Assistant CRA provides remote support for clinical trial site preparedness, monitoring activities, and site management tasks. They ensure regulatory compliance, manage study documentation, and coordinate logistics for site staff and vendor activities.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, conduct site visits, and manage documentation to maintain audit readiness.
The Technical Sales Specialist is responsible for driving sales and providing technical support for flow cytometry analyzers and cell sorters within academic, government, and industrial accounts. This role involves prospecting for new business, conducting instrument demonstrations, and representing the company at scientific trade shows and events.
The Account Executive will manage and grow revenue for the Protein Diagnostic Division by prospecting new laboratory and health system business while maintaining existing accounts. They will implement strategic sales plans, conduct instrument demonstrations, and act as a trusted advisor to customers to ensure long-term growth and satisfaction.
The Principal Operations Strategy Specialist provides expert guidance in the formulation and execution of clinical trial strategies to ensure operational efficiency and strategic alignment. They collaborate with cross-functional teams to develop budgets, manage proposal deliverables, and drive initiatives that enhance clinical trial success.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
Provides strategic leadership for clinical trial nutrition programs, including program design, implementation, and vendor management. Leads cross-functional teams to ensure regulatory compliance and operational excellence across regional and multi-site studies.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
Manage full-cycle recruitment for commercial and operations roles across Israel, the Middle East, and Africa. Collaborate with stakeholders to drive data-informed hiring strategies and process improvements.
The Clinical Sales Specialist is responsible for driving revenue growth through new business development and managing existing accounts within a specified territory. This role involves executing the full sales cycle, from lead qualification and cold calling to price negotiation and sales forecasting.
The Lead Account Manager will drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. They will build strategic relationships with key decision-makers to position the company as a preferred provider for life-changing therapies.
The Inside Sales Representative is responsible for identifying new business opportunities and managing the existing customer base within Germany. They will position product and service solutions, manage contracts, and maintain sales pipelines in Salesforce to drive revenue growth.
The Associate Contract Manager leads the review, negotiation, and finalization of contract templates and parameters while ensuring quality and risk assessment. They act as a regional interface for clients and collaborate with internal departments to facilitate site startup activities.
The Associate Site Activation Specialist manages the critical path for site activation to ensure rapid project implementation and regulatory compliance. They act as a subject matter expert, providing technical guidance and coordinating with internal departments to align site startup activities.
The Technical Sales Specialist is responsible for driving revenue growth for inorganic spectroscopy products by identifying new client opportunities and supporting account managers. They act as a technical advisor throughout the sales cycle, from prospecting to closing, while providing product expertise and training to internal teams.
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.
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 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 Customer Success Manager is responsible for selling service products, including warranty extensions and maintenance contracts, while managing customer relationships. They will also handle contract renewals, prepare sales reports, and collaborate with internal teams to achieve financial targets.
The Senior Key Account Manager is responsible for driving sales strategies and managing account activities for Life Science Electron Microscopy products within the assigned territory. They will lead sales efforts, maintain accurate booking forecasts, and build professional networks within the pharma and biotech sectors to achieve business goals.
Drive profitable sales growth by managing biotech accounts and executing territory plans across various drug modalities. Build and maintain strong customer relationships while collaborating cross-functionally to deliver integrated solutions.
The role involves providing technical and strategic leadership for CMC analytical development, including oversight of outsourced QC testing and regulatory compliance. You will manage change controls, deviations, and stability programs while contributing to global submission plans and product life cycle management.
Perform on-site installations, validations, preventive maintenance, and repairs of laboratory equipment while providing responsive technical support. Coordinate service schedules and deliver an outstanding customer experience to ensure instrument performance and customer satisfaction.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs 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 Procurement Assistant will support procurement operations and administrative tasks. The role involves managing standard office-based procurement workflows.
You will lead the Professional Services business for DSAS, overseeing revenue delivery, operational execution, and project governance. Additionally, you will collaborate with cross-functional teams to deliver comprehensive LIMS solutions while ensuring high customer satisfaction and cost control.
The Resource Analyst is responsible for forecasting, tracking, and identifying resource allocation needs and availability for clinical projects. They also coordinate project team compositions and liaise with internal departments to prioritize resourcing for future work and bid defense meetings.
Provide expert installation, maintenance, and repair services for sophisticated laboratory automation equipment and dynamic scheduler software. Build strong customer relationships while ensuring optimal system performance through preventive maintenance and user training.
Define and govern the rare disease portfolio strategy while leading high-value executive client engagements and bid defenses. Partner with cross-functional leadership to convert scientific strategy into measurable revenue, quality, and delivery outcomes.
The Senior Project Manager serves as the primary sponsor contact and is accountable for the overall delivery of global Oncology/Hematology trials regarding quality, time, and cost. They lead cross-functional teams, manage project risks, and ensure compliance with regulatory requirements and internal SOPs.
The Innovation Technologist designs and delivers end-to-end digital solutions by integrating full-stack development, data engineering, and AI/ML capabilities. They collaborate with cross-functional stakeholders to ensure solutions meet clinical, regulatory, and business requirements.
The Account Manager will develop and maintain strategic relationships with customers in the London, Ontario area to drive revenue growth. They will implement sales strategies, identify new business opportunities, and provide expert support for a portfolio of scientific products.
The Global Study Lead provides strategic and operational leadership for the end-to-end delivery of global clinical studies, with a specific focus on Managed Access Programs. They are responsible for managing study timelines, budgets, quality, and cross-functional teams while serving as the primary escalation point for clinical operations.
The Senior Technical Sales Specialist will manage and grow the sales funnel for single-use technologies within the BioProduction Group. This role involves collaborating with account managers and field application scientists to develop account strategies and drive new product adoption.
The Clinical Research Associate monitors investigator sites to ensure protocol and regulatory compliance using a risk-based approach. They are responsible for managing site documentation, verifying data accuracy, and facilitating communication between investigative sites and the project team.
Performs and coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. Manages site relationships and conducts remote or on-site visits to assess regulatory adherence and audit readiness.
The 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 Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage documentation to ensure data reliability and subject safety.
The Strategic Account Manager is responsible for driving reagent revenue growth and customer retention across a defined portfolio of laboratory accounts. They will develop strategic account plans and serve as the primary point of contact between customer stakeholders and internal commercial partners.
The Accountant II will perform monthly closing activities, including journal entries and financial analysis, while ensuring compliance with U.S. GAAP and Sarbanes-Oxley requirements. They will also drive continuous improvement in financial systems and support internal and external audit processes.
The Sr. Safety Specialist is responsible for driving sales of safety products and services within a defined territory to industrial and medical customers. They will develop sales strategies, conduct hazard assessments, and maintain strong relationships with purchasing and end-user stakeholders.
The 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 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 Regulatory Affairs Specialist will manage CMC compliance activities, including change controls, deviations, and regulatory submissions. They will collaborate with cross-functional teams to ensure product registrations and documentation meet global regulatory requirements.
The Global Regulatory Lead will develop and execute global regulatory strategies while serving as a key business partner for product life cycle management. This role involves coordinating regulatory filings, overseeing vendors, and ensuring timely compliance with global health authority requirements.
The 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.
Lead and perform complex internal and external GCP audits to ensure compliance with regulatory standards and client requirements. Prepare comprehensive audit reports and provide quality support to project teams and external clients.
The Country Approval Specialist manages and coordinates local regulatory submissions in alignment with global submission strategies. They act as the key contact for regulatory activities and ensure site start-up processes meet established timelines.
The NGS Sales Specialist will drive revenue growth by strategically selling advanced scientific instruments and managing key customer relationships across research, pharmaceutical, and industrial sectors. They will collaborate with cross-functional teams to identify opportunities and deliver customized solutions that meet customer needs.
The Senior Clinical Sales Specialist will drive revenue growth and develop new business opportunities within hospitals and laboratories. They will serve as a trusted advisor by applying a consultative approach to understand customer needs and provide tailored clinical diagnostic solutions.
The Field Service Engineer will install, maintain, 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 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 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 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 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 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 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.
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 Project Support Specialist is responsible for managing operational metrics, ensuring audit readiness, and supporting departmental process improvements. They provide end-to-end oversight of study-level activities and maintain high training compliance across functional departments.
Field Service Engineers manage customer relationships and provide technical support, including installation, repairs, and preventative maintenance of chromatography and mass spectrometry equipment. They are responsible for meeting service level agreements and internal key performance indicators while ensuring high levels of customer satisfaction.
The Field Service Engineer will conduct on-site installation, maintenance, and repair of sophisticated microscopy equipment. They will also provide technical training to customers and act as a subject matter expert for system troubleshooting and documentation.
The 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.
Drive sales growth in the clinical trials division by identifying new target clients and molecules while managing existing account relationships. Develop and implement strategic sales plans to expand market share for clinical packaging, labeling, and distribution services.
The Senior Recruiter will manage full-cycle recruitment for diverse roles while acting as a strategic talent advisor to business partners. They are responsible for developing sourcing strategies, building talent pipelines, and providing data-driven insights to hiring managers.
You will lead and support a team of field service engineers to ensure high-quality service delivery and operational excellence. The role involves coordinating service activities, managing team performance, and maintaining strong relationships with customers and internal stakeholders.
The Supervisor will lead a team of Field Service Engineers, managing their performance, development, and daily scheduling. They will also facilitate team communication, handle customer escalations, and perform field service activities for approximately 50% of their working hours.
The Country Approval Specialist manages the preparation, review, and coordination of local regulatory submissions and site start-up activities. They also lead complex site contract and budget negotiations while ensuring compliance with global and local regulatory standards.
Provide technical support, training, and scientific expertise for IC and HPLC analytical solutions to customers. Collaborate with cross-functional teams to optimize customer workflows, conduct product demonstrations, and drive business growth.
The Field Service Engineer is responsible for installing, maintaining, troubleshooting, and repairing sophisticated analytical and scientific instruments. They will provide exceptional customer service while supporting customers across research, industrial, and healthcare settings.
The Technical Sales Specialist is responsible for driving revenue growth for chromatography and mass spectrometry products by identifying new client opportunities and supporting account managers. They act as a trusted advisor to customers, managing the entire sales cycle from prospecting to closing while providing technical expertise.
The specialist will perform and oversee daily pharmacovigilance activities, including the collection, monitoring, and assessment of safety information. They will also collaborate with project teams, manage clinical study administration, and mentor less experienced staff.
You will coordinate clinical monitoring and site management processes to ensure trials adhere to protocols, ICH-GCP guidelines, and regulatory requirements. This involves conducting on-site or remote visits, managing documentation, and performing root cause analysis to mitigate risks and ensure data reliability.
The specialist will facilitate site start-up activities, including essential document collection and review to ensure study timelines are met. They will also partner with internal teams and CROs to resolve activation delays and maintain accurate eTMF records.
The Senior 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 specialist will coordinate and manage the quality of clinical translations while maintaining terminology and style guides. They will also perform quality checks on clinical documents and monitor the performance of external language suppliers using CAT technology.
Develop and implement strategic sales plans for Olink Proteomics workflows while managing key account relationships. Serve as a trusted advisor to customers through consultative selling to help them achieve their scientific goals.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage essential documentation to guarantee data reliability and subject well-being.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and the project team.
The Clinical Research Associate will monitor investigator sites to ensure protocol compliance, data accuracy, and regulatory adherence through risk-based monitoring. They will also manage site documentation, facilitate communication between stakeholders, and participate in investigator meetings and trial close-out activities.
The 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 PV Coordinator manages safety documentation, coordinates protocol inquiries, and facilitates meetings for clinical trials and safety boards. They also ensure audit readiness, perform data entry, and maintain effective communication with internal and external project stakeholders.
The Senior Safety Reporting Coordinator manages the submission, tracking, and archiving of safety reports while providing administrative support to the Pharmacovigilance department. They also lead projects, mentor team members, and ensure compliance with standard operating procedures.
The Account Manager is responsible for selling service contracts for chromatography and molecular scientific equipment within the French territory. They will focus on exceeding sales quotas, developing account-specific strategies, and collaborating with cross-functional teams to drive growth.
The Clinical Data Manager Project Manager oversees the functional, administrative, and financial aspects of clinical studies or programs. They are responsible for leading project teams, managing budgets, mitigating risks, and ensuring deliverables meet client expectations.
You will develop and implement strategic sales plans to increase revenue while managing key account relationships across the Upper Midwest. By serving as a trusted advisor, you will provide tailored scientific solutions to help customers achieve their goals.
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.
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.
Lead a field sales team to drive revenue growth and market expansion through strategic initiatives and customer relationships. Collaborate across divisions to deliver scientific solutions and achieve growth targets.
Monitor investigator sites using a risk-based approach to ensure data accuracy and compliance with protocols and regulatory requirements. Manage site initiation, close-out, and maintain regular communication with investigative sites to resolve deficiencies.
Manages day-to-day operations, resource allocation, and project timelines for the Clinical Data Management programming team. Provides technical leadership in database design and testing while overseeing staff performance and professional development.
Performs clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data reliability and maintain audit readiness.
The 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.
The role involves coordinating clinical monitoring and site management processes to ensure trial compliance with protocols and ICH-GCP guidelines. Key duties include conducting remote or on-site visits, performing data verification, and managing relationships with investigational sites.
The role focuses on completing investigator payment reconciliations in adherence to contractual guidelines and country regulations. Responsibilities include compiling patient activity data, managing bi-annual and final reconciliations, and resolving payment-related issues.
Accountable for the end-to-end operational delivery of global clinical studies, ensuring they are completed on time, within budget, and according to quality standards. This includes managing study plans, overseeing vendors, and leading matrix teams to achieve study deliverables.
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.
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.
Manages and coordinates medical projects to ensure compliance and optimal performance throughout the project lifecycle. Performs safety data reviews, manages project financials, and serves as the primary point of contact for clinical project teams.
Provide administrative and technical support for clinical trials, focusing on regulatory inspection readiness and site activation activities. Collaborate with study managers and CROs to manage study documentation, CTMS/TMF activities, and study close-out processes.
Provide administrative and technical support for clinical trials, including file reviews and system maintenance of eTMF and Activate. Coordinate site activation, regulatory submissions, and collaborate with teams to ensure project goals are met on time and within budget.
Coordinate and facilitate clinical trial activities, providing administrative and technical support to the project team. Manage study-specific documentation, perform file reviews, and act as a cross-functional liaison to ensure tasks are completed on time and within budget.
Manage and expand strategic relationships with key biopharmaceutical customers to drive revenue growth. Collaborate with cross-functional teams to align bioproduction portfolios with customer goals and ensure flawless execution.
Drive growth within health systems and laboratories by advancing the adoption of immunodiagnostic testing solutions. Orchestrate internal resources to expand testing menus and communicate clinical and economic value to senior executive stakeholders.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They act as a key country-level contact for regulatory activities and maintain accurate trial status information in tracking databases.
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.
Perform on-site installation, alignment, and repair of sophisticated electron microscopy equipment for electronics research and manufacturing clients. Provide technical support, conduct planned maintenance, and collaborate with application scientists to resolve complex system issues.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They act as a key country-level contact for regulatory activities and maintain accurate trial status information in tracking databases.
Draft, review, and negotiate agreements with study sites while ensuring compliance with budgetary and contractual parameters. Coordinate with internal functional teams to align site startup activities and achieve target cycle times for site activation.
Lead the North American commercial organization for BioProcessing to drive profitable revenue growth and market share. Develop and execute commercial strategies while managing sales operating rhythms and strengthening customer relationships.
The Lead Biostatistician serves as the statistical lead for high-profile pharmacovigilance and safety-focused projects, designing studies and developing statistical analysis plans. They provide strategic leadership for real-world evidence generation and mentor junior biostatisticians to ensure quality and accuracy.
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.
The Clinical Data Team Lead manages data management activities for clinical trials, acting as the primary liaison between the client and the project team. Responsibilities include developing project documentation, monitoring study metrics, and mentoring junior staff to ensure operational excellence.
Accountable for achieving final clinical deliverables and clean data within contractual timelines and budgets. Manages operational and quality aspects of complex clinical studies in compliance with ICH GCP guidelines.
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.
Develop and maintain direct customer relationships within the semiconductor and electronics sectors in Japan to drive sales growth. Responsibilities include creating strategic sales plans, conducting product demonstrations, and serving as a technical advisor for advanced analytical instruments.
Develop and manage the global Make/Buy strategy by designing analytical frameworks and validating site P&Ls. Lead cross-functional teams to identify cost efficiencies and optimize the manufacturing network through rigorous financial and operational analysis.
Lead the 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.
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.
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 medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, adverse events, and clinical trial deliverables such as CSRs and periodic safety reports.
Lead the collection, organization, and analysis of qualitative data to build a best-in-class qualitative research center of excellence. Manage staff, vendors, and AI-enabled technologies while developing business plans and quality assurance processes for patient-centered research.
Provide comprehensive customer support and technical leadership for FIB-SEM systems to solve physical analysis challenges and improve semiconductor yield. Responsibilities include developing automation recipes, supporting sales through PoCs, and collaborating with product development teams.
The role involves preparing and finalizing global investigator grant budgets and payment schedules for multiple studies. It also requires coordinating with clients and internal teams to align budget negotiations with site activation timelines.
The Staff Technical Sourcing Engineer develops strategies for cost savings and risk mitigation while ensuring supplier quality for electrical and electro-mechanical components. This role involves collaborating with R&D and procurement to align global sourcing strategies and managing projects through their entire lifecycle.
The specialist manages and coordinates local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. They serve as the primary country contact for regulatory activities and maintain accurate trial status tracking in databases.
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.
Manage the performance and workload of Medical Writers while overseeing the preparation and quality of regulatory deliverables. Coordinate resource planning, develop training programs, and interact with business development to prepare project proposals and budgets.
Drive business growth for Proteomic Sciences by spearheading sales engagements across academia, clinical research, and biopharmaceutical sectors. Focus on expanding the installed base, executing go-to-market strategies, and managing regional growth targets in the ANZ market.
The role involves monitoring investigator sites using a risk-based approach to ensure protocol and regulatory compliance. Responsibilities include conducting site visits, managing essential documentation, and maintaining collaborative relationships with investigative sites.
Lead strategic development engagements to align customer needs with scientific capabilities and accelerate business growth. Coordinate integrated product development plans from preclinical to post-approval while managing stakeholder relationships and resource allocation.
Perform and coordinate clinical monitoring and site management to ensure trial conduct aligns with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The role focuses on converting contract renewal quotations into purchase orders for existing customers through direct interaction via email and telephone. The specialist is responsible for achieving sales targets, upselling services, and collaborating with Customer Care Centers to ensure alignment on renewals.
The Clinical Trial Manager is responsible for achieving final clinical deliverables and ensuring clean data within contractual timelines and budgets. This includes managing operational and quality aspects of studies, developing clinical tools, and leading clinical teams in compliance with ICH GCP.
Provide internal legal support for West Europe with a focus on France, including drafting and negotiating various commercial agreements. Act as a strategic partner to leadership to implement legal processes and ensure compliance with healthcare and anti-gift laws.
Coordinate and prepare local regulatory and ethical submissions in alignment with global strategies for clinical trials. Manage site start-up activities and maintain accurate trial status information in tracking databases.
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 is responsible for monitoring and managing clinical trial sites to ensure compliance with study protocols and regulatory requirements. This includes conducting on-site and remote visits, reviewing data for accuracy, and safeguarding patient safety.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation. They conduct remote and on-site visits, perform data verification, and maintain collaborative relationships with investigative sites.
Coordinate and prepare local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. Act as the key country-level contact for regulatory activities and maintain accurate trial status tracking in databases.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol and regulatory compliance while managing site documentation. They perform risk-based monitoring, conduct site visits, and maintain collaborative relationships with investigative sites to guarantee data reliability.
The Assistant CRA performs remote activities to support site preparedness, monitoring processes, and site management in accordance with SOPs. Responsibilities include managing essential documents, coordinating study supplies, and performing data reconciliation tasks.
Identify and develop new business opportunities while nurturing customer relationships to drive market growth. Provide innovative scientific product solutions and collaborate with cross-functional teams to advance research and healthcare outcomes.
The Clinical Trial Manager is responsible for achieving final clinical deliverables and clean data within contractual timelines and budgets. This includes managing operational and quality aspects of studies, developing clinical tools, and leading clinical teams in compliance with ICH GCP.
Perform clinical monitoring and site management to ensure trial conduct aligns with protocols, ICH-GCP guidelines, and regulatory requirements. Conduct remote and on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites.
The role involves preparing and coordinating local regulatory and ethical submissions in alignment with global strategies to ensure timely site activation. It also includes managing trial status tracking, maintaining study files, and collaborating with internal departments and investigators.
The role involves monitoring investigator sites to ensure protocol and regulatory compliance using a risk-based approach. Responsibilities include conducting site visits, managing essential documentation, and facilitating communication between sites and sponsors.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring activities. Coordinate site management tasks, document collection, and system access in accordance with SOPs and regulatory guidelines.
Provide medical leadership and support for clinical trials, including the creation of protocols and real-time medical monitoring of study subjects. Serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and safety.
Perform periodic maintenance, troubleshooting, and installation of electron microscopes and X-ray photoelectron spectrometers. Collaborate with sales teams to plan equipment layouts and provide technical support to customers.
Perform periodic maintenance, troubleshooting, and installation of electron microscopes and analytical devices. Collaborate with sales teams to plan equipment layouts and specifications for customer sites.
Provides medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Responsible for medical review of safety data, serious adverse events, and the preparation of periodic safety reports.
Drive testing initiatives for generative AI and clinical trial technology using advanced manual testing practices. Design and execute test cases, perform API and integration testing, and validate data using SQL queries.
Lead the drafting, negotiation, and finalization of clinical trial agreements and investigator budgets. Collaborate with sites, sponsors, and legal teams to ensure efficient site activation and risk mitigation.
Coordinate site activation and regulatory submissions to ensure clinical trials are initiated efficiently and in compliance with local regulations. Partner with cross-functional teams to manage submission strategies, site documentation, and start-up timelines.
Lead the operational delivery of clinical studies from start-up through closeout, ensuring quality, compliance, and adherence to timelines. Manage cross-functional teams, oversee Trial Master File quality, and maintain strong communication with sponsors and investigative sites.
The Senior CRA is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting remote and on-site visits, managing essential documentation, and maintaining collaborative relationships with clinical sites.
The Lead Data Engineer is responsible for designing, building, and maintaining scalable data pipelines and platforms to support business operations. This includes optimizing data models, ensuring data governance, and collaborating with analytics teams to meet data requirements.
Lead the design and implementation of robust bioanalytical strategies within a client-dedicated global biopharma team. Coordinate with lab-based scientists and regulatory agencies to mitigate risk and submit necessary documentation.
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.
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.
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).
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.
The Site Contract Specialist is responsible for drafting, negotiating, and finalizing clinical trial agreements and budgets with study sites. They collaborate with internal teams and CROs to ensure quality, objectivity, and timely delivery of contracts while adhering to fair market value guidance.
Ensure compliance with global regulations by interpreting guidelines and developing regulatory strategies for innovative products. Support the entire product lifecycle and improve regulatory information systems to enable business growth and patient safety.
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.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage strategic accounts and build executive-level relationships to position the company as a preferred provider.
Drive sales growth and customer success for advanced analytical instruments across diverse markets including pharmaceutical and environmental sectors. Manage the full sales cycle from identifying opportunities and providing quotations to negotiating contracts and maintaining account pipelines.
The Technical Sales Specialist is responsible for driving revenue growth of instrument and consumables portfolios within the Chromatography and Mass Spectrometry Division. This involves managing the full sales cycle from prospecting to closing while acting as a technical advisor to customers and account managers.
The QC Coordinator manages the assignment and tracking of quality check requests for translation projects with internal and external linguists. They are responsible for maintaining delivery schedules, managing client communications, and recording KPI data for business analysis.
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, including serious adverse events and periodic safety reports across the product life-cycle.
Design and manage secure, scalable, multi-tenant database architectures for a healthcare SaaS platform. Ensure strict compliance with healthcare regulations like HIPAA and GDPR while optimizing performance for large-scale datasets.
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.
The role involves coordinating clinical monitoring and site management, including source data verification and ensuring protocol and regulatory compliance. It requires conducting on-site and remote visits while collaborating with cross-functional teams to maintain audit readiness.
Manage and coordinate local regulatory and ethical submissions to support clinical trial startup in alignment with global strategies. Act as the primary country-level contact for site activation and maintain accurate trial status tracking databases.
Manages the preparation and coordination of country-specific regulatory submissions in alignment with global strategies. Serves as the primary contact for investigators and regulatory authorities to ensure timely site activation and compliance.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage strategic accounts and build executive-level relationships to position the company as a preferred provider.
Perform and coordinate all aspects of the clinical monitoring process independently. Provide end-to-end support for clinical trials from study start-up through to close-out.
Provide medical leadership and support for clinical trials in nephrology, including protocol creation and real-time medical monitoring. Act as the primary medical liaison between the sponsor and internal departments to ensure subject safety and study compliance.
Install, maintain, and repair sophisticated electron microscopy systems including SEM, TEM, and FIB instrumentation. Provide technical support to customers, conduct preventive maintenance, and ensure optimal system performance through complex troubleshooting.
The Clinical Data Team Lead manages end-to-end external data acquisition activities, including vendor integrations and data ingestion for clinical studies. They act as a liaison between departments and clients while ensuring all data management deliverables are audit-ready and compliant with regulatory standards.
The Regulatory Affairs Manager will lead the preparation of global clinical trial submissions and provide strategic regulatory guidance to internal and external clients. They are responsible for overseeing multiple projects, managing budgets, and ensuring high-quality regulatory performance across the clinical development lifecycle.
The Senior Clinical Trial Manager is responsible for managing all clinical operational and quality aspects of studies to ensure deliverables meet time, quality, and cost expectations. They lead clinical teams, oversee project financials, and ensure compliance with ICH GCP and regulatory standards.
The 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 Process Instrument Sales Representative will lead all aspects of the sales process for Molecular Spectroscopy process instruments in a multi-state western region. Responsibilities include coordinating technical interactions, delivering product demonstrations, and meeting sales goals.
Provide medical leadership to study teams, including creating clinical trial protocols based on the latest scientific information and contributing to document review and approval. Perform real-time medical monitoring of clinical studies to ensure medical validity and subject safety, while identifying and escalating medical issues early.
The Clinical Research Associate (Level II) will conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure trials adhere to approved protocols, ICH-GCP guidelines, and SOPs. Key duties include monitoring investigator sites using a risk-based approach, performing data review, assessing investigational product, documenting observations, and escalating deficiencies to management.
This role involves ensuring high-quality input into significant requests for proposals, including strategy, regulatory issues, and protocol considerations for cardiovascular indications. The incumbent will also support proactive client engagement, develop product plans through consulting, provide therapeutic expertise to internal teams, and contribute to innovative initiatives.
Provide medical leadership to study teams and ensure the medical validity of clinical studies. Contribute to the creation and review of clinical trial protocols and ensure compliance with medical aspects.
The Principal CRA will lead and coordinate all aspects of clinical monitoring and site management for complex trials, ensuring adherence to protocols, ICH-GCP, and regulatory requirements while acting as a subject-matter expert and escalation point. Key duties involve leading monitoring activities, performing site visits, overseeing data review, managing essential documents, and driving corrective actions.
The Clinical Compliance Manager leads the assessment and classification of serious breaches in clinical trials and serves as the primary contact for breach investigations. This role also involves preparing notifications for regulatory authorities and developing standard operating procedures related to breach management.
The Senior Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management, ensuring compliance with protocols and regulations. They develop relationships with investigational sites and ensure audit readiness while documenting observations and resolving issues.
The Senior Clinical Research Associate performs and coordinates all aspects of clinical monitoring and site management, ensuring compliance with protocols and regulations. They develop relationships with investigational sites and manage documentation while conducting remote or on-site visits.
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.
