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For our client, an innovative and dynamic bio-pharmaceutical company covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, we are looking for a eTMF Specialist Regulatory Affairs for a 24‑month contract (with possibility of extension) based in Basel area, Switzerland.

The eTMF Specialist, Regulatory Affairs is responsible for the maintenance, quality, and inspection readiness of the electronic Trial Master File (eTMF) documents owned by Regulatory Affairs. The role ensures eTMF-relevant regulatory documentation is complete, accurate, timely, and compliant with applicable regulations and internal procedures. This position acts as the Regulatory Affairs ...