Senior Clinical Data Manager

As a Senior Clinical Data Manager, you will lead and oversee the full lifecycle of clinical data management activities across international studies, ensuring data quality, integrity, regulatory compliance, and cross‑functional collaboration.

You will serve as a key point of contact for internal teams and sponsors, driving strategic data decisions, mentoring junior data managers, aiding in process reviews, contributing to SOP development, and fostering clear communication across the team.

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

• Lead data management activities from study start‑up through database lock, ensuring alignment with GCP‑Service or Sponsor SOPs, ICH/GCP guidelines, and applicable national regulations.
• Mentor and support junior data managers, contributing to team development and knowledge sharing.
• Oversee the design, testing, and validation of clinical trial databases and electronic data capture (EDC) systems.
• Review and interpret clinical trial protocols to define data collection requirements and ensure protocol compliance.
• Manage data cleaning, discrepancy resolution, and quality control processes to ensure timely and accurate data delivery.
• Collaborate with cross‑functional teams (e.g., biostatistics, medical monitoring, pharmacovigilance) to support risk‑based decision‑making.
• Provide input on data management plans, risk‑based monitoring strategies, and process improvements.
• Contribute to the review and refinement of internal processes and workflows.
• Assist in drafting, reviewing, and updating standard operating procedures (SOPs).
• Communicate effectively with sponsors, clients, and internal teams regarding project status, timelines, and critical data issues.

Requirements

• Bachelor’s or Master’s degree in Life Sciences, Biostatistics, Computer Science, or a related field.
• Excellent organizational and communication skills.
• Proficiency in Microsoft Office.
• Strong understanding of clinical trial processes, regulatory requirements, and data standards.
• Proficiency in clinical data systems (e.g., Viedoc).
• Fluent in English and preferably in German (written and spoken).

Preferred Experience

• Ability to manage multiple studies and prioritize tasks in a fast‑paced environment.
• Familiarity with risk‑based study planning.
• Knowledge of eCRF design and validation best practices.

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

If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date: