Clinical Data Manager

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 trial databases, data flow, and (e)CRF design
• Familiarity with ICH-GCP and international clinical research regulations
• Strong organizational skills and a collaborative mindset
• Fluent in written and spoken English