IVDR Study Start-Up Lead – Clinical Sites

F. Hoffmann-La Roche AG seeks a Lead Clinical Site Manager specializing in In‑Vitro Diagnostics Regulation (IVDR). In this role, you will design, plan, and conduct activities for initiating and monitoring clinical research studies.

You will lead study start-up activities, manage regulatory submissions, and provide CRO oversight, ensuring efficient trial launches and compliance. A degree in a scientific discipline is required along with direct experience in clinical operations.

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