Main Responsibilities:
Lead all Data Management activities across clinical trials. Manage timelines from study setup to database lock and archiving. Provide input into protocol, CRF design, SAP, and Clinical Study Reports. Oversee data review, cleaning processes, and quality control activities Coordinate testing and implementation of data capture systems (eCRF). Manage vendors including selection, oversight, and budget review. Set goals and manage performance of direct reports. Ensure proper documentation, auditing readiness, and archiving. Qualifications and Experience:
Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required. Master’s degree in life sciences, statistics, mathematics, informatics, or related field. Minimum 5+ years experience in clinical data management within pharma/biotech sector. Strong experti...