Urgently Hiring Remote Jobs at Thermo Fisher Scientific – Medical Writer, Clinical Data Associate, Data Analyst & Senior CRA Roles
Through its PPD clinical research portfolio and global scientific teams, Thermo Fisher Scientific supports major pharmaceutical companies, biotechnology organizations, clinical trials, laboratory services, digital research models, and decentralized clinical trial solutions. These opportunities provide a strong career path for professionals seeking international exposure, structured work contracts, scientific excellence, regulatory compliance, and long-term professional growth in healthcare, life sciences, and clinical operations.
Available Remote and Flex-Remote Jobs
- Medical Writer – Medical and scientific writing, client communication, SOP compliance, timelines, budgets, and deliverables.
- Clinical Data Associate III – Clinical data support, lab database administration, trial documentation, and data quality.
- Data Analyst III – Flex remote data analysis role supporting the Drug Product Division in Ridgefield, New Jersey.
- Senior Clinical Research Associate Level I – Clinical monitoring, site management, remote and on-site visits, and regulatory compliance.
- Field Application Scientist – Upstream bioproduction, bioprocessing support, single-use technologies, and European scientific collaboration.
Job 1: Medical Writer
The Medical Writer role provides high-quality medical and scientific writing support from planning and coordination through delivery of final drafts to internal and external clients. This role is suitable for candidates with strong writing ability, scientific knowledge, medical communication skills, and experience working with regulated documentation.
The selected candidate may serve as a primary writer for routine deliverables such as medical information documents. This remote medical writing opportunity is ideal for professionals who understand SOPs, work instructions, quality processes, document requirements, and operational excellence in healthcare and scientific communication.
Medical Writer Responsibilities
- Create and review medical and scientific writing deliverables for internal and external clients.
- Support effective communication across medical, clinical, regulatory, and operational teams.
- Ensure compliance with applicable SOPs, work instructions, quality processes, and document standards.
- Assist in identifying best practices to achieve optimal writing quality and delivery results.
- Support program management tasks such as timelines, budgets, deliverable tracking, and metrics reporting.
- Contribute to medical information documents, scientific communication, regulatory clarity, and client-ready final drafts.
Job 2: Clinical Data Associate III
The Clinical Data Associate III role supports meaningful global work that contributes to clinical research, healthcare improvement, and the delivery of life-changing therapies. Thermo Fisher Scientific provides teams with resources to achieve individual career goals while advancing research, development, and clinical trial delivery.
This role is strongly connected to clinical data quality, laboratory database administration, trial documentation, and operational accuracy. The company has supported the top 50 pharmaceutical companies and more than 750 biotechnology organizations across thousands of clinical trials in more than 100 countries, making this a valuable opportunity for professionals interested in clinical data operations and global healthcare impact.
Clinical Data Associate III Responsibilities
- Support clinical trial data processes with accuracy, quality control, and documentation discipline.
- Assist with lab database administration under close supervision and according to project requirements.
- Contribute to clinical research operations across laboratory, digital, and decentralized trial services.
- Maintain reliable data practices that support better health outcomes for patients and communities.
- Work with clinical teams to ensure documentation quality, system accuracy, and operational consistency.
- Support data management, clinical reporting, regulatory readiness, and scientific research workflows.
Job 3: Data Analyst III – Flex Remote
The Data Analyst III role is a flex remote position connected to Thermo Fisher Scientific’s Ridgefield, New Jersey location. This position supports the Drug Product Division and offers candidates the opportunity to work in a dynamic environment focused on innovation, collaboration, and scientific problem-solving.
This role is suitable for data professionals who want to support solutions for major global challenges, including healthcare innovation, environmental protection, food safety, and cancer research. Candidates with experience in analytics, reporting, business intelligence, data governance, quality metrics, and cross-functional communication may find this role especially valuable.
Data Analyst III Responsibilities
- Analyze business, operational, scientific, or manufacturing data to support decision-making.
- Create clear reports, dashboards, and insights for stakeholders across the Drug Product Division.
- Support data accuracy, trend analysis, performance monitoring, and quality improvement initiatives.
- Collaborate with teams in a flex remote environment while supporting Ridgefield, New Jersey operations.
- Help develop data-driven solutions for healthcare, research, food safety, and environmental challenges.
- Contribute to operational excellence, reporting discipline, and measurable business performance improvement.
Job 4: Senior Clinical Research Associate Level I
The Senior Clinical Research Associate Level I role is designed for clinical research professionals who want to work at the forefront of innovation. This opportunity involves performing and coordinating clinical monitoring and site management activities across sponsor environments such as FSO, FSP, government programs, and other clinical trial models.
The Senior CRA will conduct remote or on-site visits to assess protocol compliance, regulatory compliance, and site documentation. This role is essential for protecting subject rights, ensuring patient well-being, supporting reliable clinical data, and maintaining audit readiness under ICH-GCP guidelines, applicable regulations, SOPs, and approved protocols.
Senior Clinical Research Associate Responsibilities
- Perform clinical monitoring and site management activities using a risk-based monitoring approach.
- Conduct remote or on-site visits to assess protocol compliance and regulatory documentation.
- Apply root cause analysis, critical thinking, and problem-solving to identify site process issues.
- Ensure clinical trials follow ICH-GCP guidelines, sponsor requirements, applicable regulations, and SOPs.
- Maintain audit readiness and develop strong collaborative relationships with investigational sites.
- Support patient safety, subject rights, data reliability, clinical quality, and trial documentation standards.
Job 5: Field Application Scientist – Upstream
The Field Application Scientist role supports Thermo Fisher Scientific’s BioProduction Group, which provides innovative solutions for bioproduction and bioprocessing. This position is especially relevant for candidates with scientific, technical, or application support experience in biopharmaceutical manufacturing, vaccines, and cell and gene therapy.
Within the Single-Use Technologies Division, the role supports disposable bioprocessing equipment and systems that help modern pharmaceutical manufacturers increase flexibility, reduce cross-contamination risks, and improve production efficiency. Candidates in Germany and broader European remote locations may benefit from strong exposure to global bioproduction innovation.
Field Application Scientist Responsibilities
- Support upstream bioproduction and bioprocessing applications for customers and internal teams.
- Provide scientific and technical support for single-use technologies and biopharmaceutical manufacturing systems.
- Help customers improve efficiency, flexibility, and quality in drug manufacturing processes.
- Collaborate with European teams to address customer needs in Germany and other markets.
- Support products and services related to vaccines, biopharmaceuticals, and cell and gene therapies.
- Contribute to scientific innovation, technical training, customer success, and long-term account development.
Other Remote Opportunities Mentioned
- FSP Senior Medical Writer – EMEA – United Kingdom remote role.
- Senior Medical Writer, Publications – France remote role.
- CRA Level II – Beijing, China remote role.
- FSP CRA Level II – Shanghai, China remote role.
- CRA I/II/Sr CRA – FSP UK – United Kingdom remote role.
- Study Manager – FSP – Poland and Bulgaria remote roles.
- Medical Science Liaison – United Kingdom remote role.
- Country Approval Specialist FSP – Italy, France, and Spain focused role.
- Senior Account Manager, Clinical Diagnostics NGS – Germany remote role.
- FSP Principal Medical Writer – Germany remote role.
General Requirements
- Relevant experience in medical writing, clinical research, clinical data, data analysis, life sciences, healthcare, bioproduction, or scientific support.
- Strong understanding of regulated environments, SOPs, quality processes, documentation standards, and client communication.
- Ability to work remotely or flex-remotely with accountability, accuracy, and professional discipline.
- Strong written and verbal communication skills for internal teams, external clients, sponsors, and stakeholders.
- Knowledge of clinical trials, ICH-GCP, regulatory compliance, data reliability, and audit readiness is highly valuable for CRA and clinical roles.
- Technical or scientific knowledge in pharmaceuticals, biotechnology, diagnostics, bioprocessing, or healthcare is preferred for specialist roles.
Benefits and Career Advantages
- Remote and flex-remote opportunities with a global science and healthcare leader.
- Exposure to pharmaceutical companies, biotechnology organizations, clinical trials, laboratory services, and decentralized research models.
- Strong professional career path in medical writing, clinical research, data analysis, regulatory support, and life sciences.
- Potential access to competitive compensation, professional employment contracts, health insurance, retirement plans, paid time off, and structured benefits according to company policy.
- Opportunities to contribute to life-changing therapies, drug development, cancer research, food safety, environmental protection, and global health outcomes.
- Valuable experience with international teams, scientific innovation, operational excellence, and regulated quality systems.
Featured Remote Locations
- United Kingdom: FSP Senior Medical Writer, Medical Science Liaison, CRA I/II/Sr CRA roles.
- France: Senior Medical Writer, Publications and Country Approval Specialist opportunities.
- Germany: Field Application Scientist, Senior Account Manager, and Principal Medical Writer roles.
- China: CRA Level II and FSP CRA Level II roles in Beijing, Shanghai, and Zhejiang.
- Poland and Bulgaria: Study Manager FSP remote opportunities.
- Mexico: CRA Level II remote opportunity.
- United States: Data Analyst III flex remote role connected to Ridgefield, New Jersey.
How to Apply
Interested candidates can apply through the official LinkedIn job listings using the application link below. Applicants should prepare a professional CV highlighting relevant medical, scientific, clinical, regulatory, writing, data analysis, or life sciences experience. For stronger consideration, include measurable achievements, therapeutic area knowledge, clinical trial exposure, SOP compliance experience, remote work discipline, and client-facing communication skills.
Application Link: Apply Now via LinkedIn