[Hiring] Sr Clinical Data Analyst @Fortrea

Role Description

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.

• 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.

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.

Benefits

• 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.

Company Description

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.