
Clincal Data Lead
- Baar, Zoug
- CDI
- Temps-plein
In this pivotal role, you will oversee outsourced data management activities, ensure inspection-ready clinical trial data, and support successful regulatory submissions.Key responsibilities:
- Lead sponsor data management deliverables from study start-up to database lock
- Oversee CRO and vendor activities, ensuring high-quality, compliant data
- Maintain oversight of third-party data sources (labs, imaging, ePRO)
- Align data review strategies with the Clinical Study Team (CST)
- Review and approve study-specific Data Quality Documentation (DQD)
- Bachelor's in Life Sciences, Health Informatics, Computer Science, or related field
- 5+ years of clinical data management experience, incl. 2-3 years in a lead role
- Proficiency with EDC systems and knowledge of CDISC standards, GCP, and regulatory requirements
- Strong communication and collaboration skills across cross-functional teams