Main Responsibilities:
Ensure Data Management activities comply with internal standards and regulatory requirements Support the development and testing of (e)CRFs and data review tools Contribute to the creation of Data Management documentation Perform data review, discrepancy and query management, and protocol deviation tracking Assist in database lock activities and provide metrics to the Project Data Manager Archive study documentation in accordance with guidelines Qualifications and Experience:
Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required; A 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 tr...