* 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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