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.

If you are interested, send us your electronic application (with your salary expectations and earliest start date) and your CV to:

E-mail: application@gcp-service.com