Clinical Data Manager

About the role

As a Clinical Data Manager you will ensure the accuracy, quality, and integrity of clinical trial data across complex global studies, supporting efficient trial execution and high‑quality deliverables.

Key responsibilities

• Lead and oversee data management activities from study start‑up through closeout for multiple global studies.
• Coordinate resources to meet deliverables on time and within budget.
• Develop and maintain trial documentation such as data management plans, database specifications, and edit check specifications.
• Drive user acceptance testing to support high‑quality database builds.
• Manage vendor data reconciliation and define output specifications.
• Oversee data cleaning to ensure accurate and reliable trial data.
• Monitor study progress, identify risks, and communicate concerns to leadership.
• Represent Data Management in study meetings and cross‑functional discussions.
• Participate in process reviews and continuous improvement initiatives.

Required profile

• Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or related discipline, or equivalent experience.
• Minimum 3 years of experience in clinical data management within pharma, biotech, or medical device industries.