Globally operating pharmaceutical company
24 months contract with take-over option
About Our Client For our client, a globally renowned pharmaceutical company in the Basel area, we are seeking a Clinical Data Manager (a) to strengthen the team in 2026 in support of Phase 3 development activities. The contract duration is 24 months with a strong take-over possibility. Hybrid work model (3 days onsite, 2 days HO.)
Job Description The Clinical Data Manager (a) will accompany and drive the phase 3 drug development by:
Ensuring Data Management activities comply with internal standards and regulatory requirements
Supporting the development and testing of (e)CRFs and data review tools
Contributing to the creation of Data Management documentation
Performing data review, discrepancy and query management, and protocol deviation tracking
Assisting in database lock activities and providing metrics to the Project Data Manager
Archiving study documentation in accordance with guidelines
The Successful Applicant To be considered for this role, you must bring:
Bachelor's degree or higher in a pharmaceutical or biomedical discipline (e.g., Biological Sciences, Pharmacology)
Minimum 2 years of experience in Clinical Research or Clinical Data Management within the Pharmaceutical or Biotech industry
Solid understanding of clinical trial databases, data flow, and (e)CRF design
Familiarity with ICH-GCP and international clinical research regulations
Strong organizational skills and a collaborative mindset
Fluency in written and spoken English
What’s on Offer The selected candidate will be part of a dynamic team in an international environment and actively contribute to shape, develop, and drive the market authorization of innovative drugs. Hybrid work model. Extension or take-over possibility.
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