Team Lead Clinical Data Management

Location: Bremen, Germany (office-based position)

As Team Lead Clinical Data Manager, you will oversee high ‑quality clinical data management in line with GCP Service‑or Sponsor SOPs, ICH/GCP guidelines, and national regulations. You will lead a team of Clinical Data Managers and manage all data r‑elated activities across international clinical studies.

Responsibilities

• Lead, mentor, and provide expert support to the Clinical Data Management team.
• Provide structured, solution-oriented leadership and foster collaboration.
• Oversee data management activities across multiple studies, ensuring accuracy, consistency, and regulatory compliance.
• Review and approve data management deliverables as per clinical trial protocols.
• Supervise the design, testing, and implementation of clinical trial databases and data entry systems.
• Ensure timely processing, tracking, validation, and reporting of clinical data.
• Coordinate data submissions and ensure audit and inspection readiness.
• Act as the primary contact for clients on data management topics.
• Collaborate with cross‑functional teams to support timelines and quality standards.
• Drive process improvements and contribute to SOP development.

Requirements

• University degree in Biology, Mathematics, Biostatistics, Computer or Health Sciences, or equivalent.
• Several years of clinical data management experience including proven leadership or team‑leading experience.
• Strong organizational, communication, and problem-solving skills.
• Proficiency in Microsoft Office.
• Fluent in English and German (written and spoken).
• Office‑based role located in Bremen.
• Experience across multiple clinical trial phases.
• Database management skills and proficiency in programming (e.g., R, Python, MySQL).
• Familiarity with eCRF programs and clinical data management systems.
• Experience in an international CRO or pharmaceutical environment.
• Experience with audits or inspections related to clinical data management.
• Ability to optimize processes and contribute to SOP improvements.