Clinical Data Manager in Bremen

Our Clinical Data Managers ensure high-quality clinical data management according to GCP-Service or Sponsor SOPs, ICH/GCP guidelines, and national regulations. In this role, you will oversee data management processes from project initiation to completion in an international setting.

Responsibilities:

• Ensure data accuracy, consistency, and compliance with federal regulations, GCP, and internal SOPs.
• Manage and review clinical trial protocols.
• Design and test clinical trial databases and data entry systems.
• Process, track, and validate clinical data accurately and on time.
• Develop and generate patient clinical data reports.
• Assist in creating project-specific reports and submitting clinical data for monitoring.
• Communicate with clients regarding project status and key issues.

Requirements:

• Bachelor’s degree in STEM (Science, Technology, Mathematics) or Health Sciences, or an equivalent qualification.
• Proficiency in Microsoft Office.
• Strong organizational, communication, and computer skills.
• Fluent in English and German (written and spoken).
• This role is suitable for candidates with 0-3 years of professional experience (junior level), as well as career changers or side entrants with strong programming skills and an interest in clinical research and data analysis.

Preferred Experience:

• Experience in clinical trial data management.
• Database management skills with proficiency or interest in programming (R, Python, MySQL).
• Familiarity with eCRF programs and data management systems.

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