Sr Clinical Data Analyst - Medical Device

Fortrea is looking for a Sr Clinical Data Analyst (2–4 years’ experience) to join our medical device team As a Sr Clinical Data Analyst at Fortrea, you will play a key role in ensuring the quality, integrity, and timeliness of clinical trial data across assigned studies. Working alongside a diverse group of research professionals, you will collaborate closely with cross-functional project teams to support database set-up, ongoing data review, and database lock—always aligned with protocol requirements, global harmonized SOPs, and applicable GCP standards.

• Your Responsibilities:
• Ensure all allocated projects are delivered in strict accordance with protocols, global harmonized SOPs, and applicable GCP standards.
• Perform clinical data management activities including data review and query management, ensuring quality standards (internal and client) are met within agreed timelines.
• Generate, resolve, and track queries arising from aggregate data review activities.
• Run and execute additional programs and outputs (e.g., special listings, reconciliation discrepancy listings, and other outputs supporting data review).
• Partner with study team members to support set-up, maintenance, and close-out of Data Management project activities; attend meetings as required.
• Assist with—or create—dummy data to test edit checks, database screen design/functionality, and SAS reports/data listings.
• Support the team by preparing study forms/memos and completing data management documentation and administrative activities, including eTMF maintenance when required.
• Generate study status reports and perform database extracts.
• Assist with Database Lock activities and contribute to inspection/audit readiness.
• Your experience and qualifications:
• University/college degree in life sciences, health sciences, information technology, or a related discipline (or a certification in allied health professions from an accredited institution).
• Fluent in English, written and spoken.
• 2 to 4 years of applicable experience in clinical research (Data Management preferred); additional relevant experience may substitute for education requirements.
• Hands-on experience with clinical EDC platforms.
• Knowledge of medical terminology.
• Strong time management skills with the ability to work to productivity metrics and timelines.
• Solid understanding of effective clinical data management practices.
• What you can expect from us:
• Pioneering Research: Join a global CRO supporting clinical trials across multiple therapeutic areas.
• Career Growth: Expand your skill set in a supportive environment with opportunities for development and progression.
• Impactful Work: Help deliver high-quality data that supports the development of life-changing therapies and treatments.
• Competitive Compensation: A competitive salary package, comprehensive benefits, and a rewarding bonus structure.
• Life-Style: Flexibility to work remotely (role/location dependent), supporting a healthy work-life balance.

You can be 100% home-based in any of the EMEA locations listed on this ad.

• Fortrea is a leading global clinical research organization (CRO) with decades of experience and a global footprint—working to help move clinical trials forward and make delivery easier for sponsors, sites, and patients.
• For more information about Fortrea, visit www.fortrea.com.
• Fortrea is proud to be an Equal Opportunity Employer:
• As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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