We offer an exceptional opportunity for a professional in Allschwil (Basel-Land) seeking a new challenge and responsibility in a well-established international pharmaceutical organization with a strong focus on clinical development, data quality, and patient safety. This organization operates globally across branded medicines, generics, and complex therapies and is committed to improving access to high-quality healthcare worldwide.
As a Data Manager, you will play a key role in ensuring the accuracy, integrity, and compliance of clinical trial data. You will join a collaborative, cross-functional clinical team and contribute directly to the successful execution of international clinical studies.
Role Description
* Ensure Data Management activities comply with internal standards and regulatory requirements (e.g., ICH-GCP)
* Support the development and testing of (e)CRFs and data review tools
* Contribute to the creation and maintenance of Data Management documentation
* Perform data review, discrepancy and query management, and protocol deviation tracking
* Assist with database lock activities and provide metrics to the Project Data Manager
* Archive study documentation in accordance with guidelines
Your Profile
* Bachelor's degree or higher in a pharmaceutical, biomedical, or life sciences discipline
* Minimum 2 years of experience in Clinical Research or Clinical Data Management
* Solid understanding of clinical trial databases, data flow, and (e)CRF design
* Familiarity with ICH-GCP and international clinical research regulations
* Fluent in written and spoken English
* Strong organizational skills and a collaborative mindset
If you are an experienced Data Manager looking to make a meaningful impact in clinical development, we encourage you to apply.
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