Job Description
Turn safety data into smarter decisions that protect patients worldwide.
Proclinical is seeking an Associate Safety Director to join a dynamic team in Switzerland. This role focuses on providing safety science and pharmacovigilance expertise across the drug development lifecycle, from early-phase studies to post-market activities. You will play a key role in ensuring the safety of assigned products, contributing to regulatory submissions, and managing risk strategies.
This position offers a hybrid work model following an initial training period.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities
- Develop and maintain a deep understanding of the safety profile of assigned products or therapy areas.
- Oversee individual and aggregate case reporting activities, including ICSR case management, medical review, and DSUR/PBRER reporting.
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Submit your application today and join our talented team at Proclinical Group.
Submit ApplicationJob Details
- Location basel, basel stadt
- Job Type Full-time
- Category Management & Operations
- Posted Date June 23, 2026
- Application Deadline August 02, 2026