EINFÜHRUNGData 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. AUFGABENBESCHREIBUNGEnsure 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 toolsContribute to the creation and maintenance of Data Management documentationPerform data review, discrepancy and query management, and protocol deviation trackingAssist with database lock activities and provide metrics to the Project Data ManagerArchive study documentation in accordance with guidelinesERFORDERLICHES PROFILBachelor's degree or higher in a pharmaceutical, biomedical, or life sciences disciplineMinimum 2 years of experience in Clinical Research or Clinical Data ManagementSolid understanding of clinical trial databases, data flow, and (e)CRF designFamiliarity with ICH-GCP and international clinical research regulationsFluent in written and spoken EnglishStrong organizational skills and a collaborative mindsetIf you are an experienced Data Manager looking to make a meaningful impact in clinical development, we encourage you to apply. jid37b0baca jit0105a jiy26a