Team Lead Clinical Data Management
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.
SUBMIT 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 [email protected].
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.
SUBMIT 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 [email protected].
We wish you all the best in your job search.
Best regards,
HR team @ GCP Service International
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