Clinical Data Manager

GCP-Service International; Bremen; On-site; EUR 40,000 - 60,000; Full time

Job summary

GCP-Service International is seeking a Clinical Data Manager to oversee data management across the full lifecycle of clinical trials in an international setting. The role requires collaboration with sponsors and adherence to GCP and national regulations.

The candidate should have a STEM or Health Sciences background, fluent English and German, and strong data analysis and programming interest. This entry-level position welcomes junior candidates with 0–3 years of experience and programming

Qualifications

• Bachelor’s degree in STEM or Health Sciences or equivalent.
• Strong organizational and communication skills.
• Fluent in English and German (written and spoken).
• Interest in clinical research and data analysis; junior level (0–3 years) possible.

Responsibilities

• Ensure data accuracy and regulatory compliance (GCP, SOPs).
• Oversee data management processes from initiation to completion in an international setting.
• 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 submissions for monitoring.
• Communicate project status and issues to clients.

Education

Bachelor’s degree in STEM or Health Sciences

Tools

Microsoft Office

Job description

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.