Team Lead Clinical Data Management
- GCP-Service International
- Anne-Conway-Straße 2, 28359 Bremen, Germany
- 17/04/2026
Job Description
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 (eg, 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.
If you are interested in joining our team, please use the link below to submit your application.
Thank you for submitting your application. We truly appreciate your interest in joining our company.
Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.
In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.
If you have any questions regarding data protection, please contact our Data Protection Officer at dataprotection@gcp-service.com.
We wish you all the best in your job search.
Best regards,
HR team @ GCP Service International
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 (eg, 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.
If you are interested in joining our team, please use the link below to submit your application.
Thank you for submitting your application. We truly appreciate your interest in joining our company.
Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.
In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.
If you have any questions regarding data protection, please contact our Data Protection Officer at dataprotection@gcp-service.com.
We wish you all the best in your job search.
Best regards,
HR team @ GCP Service International
GCP-Service is a privately owned full-service CRO. Since its foundation in 2004, the company has grown to a size that enables it to deliver all required services, while maintaining high flexibility and minimising overhead costs. This provides GCP-Service with the scope to conduct a wide variety of clinical studies, meeting the individual and specific needs of our clients. Mission: We are convinced that the multiple innovative processes as well as competence and continues development of our employees provide unique advantages during the conduct of clinical studies to our company, to our clients, to our partners and to our vendors. Our daily business is based on our company values: 1. Respect, acceptance and tolerance are the basis of a positive working environment 2. We think that trust builds sustainability, stability and creativity 3. We reach high grade of satisfaction by our flexibility 4. Reliability is the foundation of our service provisions 5. Fair and honest interaction are the basis of our interpersonal relationships 6. Continuous professional and personal development let us achieve and exceed expectations Our values are our strength which constitute the basis of our success and the success of our clients, partners and vendors. "We do not want to be the biggest CRO, but we want to be the best CRO, which provides the highest value to our clients! Our clients are organizations which believe that “people are working with people”, but not just “companies with companies”. (CEO, Dr Andreas Grund)