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 Biology, Mathematics, Biostatistics, Computer 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).

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.

Clinical Data Manager (m/f/d)