Job Description

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...

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