Data Manager
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.
Responsibilities
* 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
Qualifications
* 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.
#J-18808-Ljbffr