Senior Medical Writer

Lausanne, Vaud, Switzerland · Clinical Research & Development


The Senior Medical Writer develops study protocols and amendments, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), Investigator's Brochures (IBs) and other regulatory documents for our Oncology programs, ensuring compliance with international requirements. He/she manages the process of reviews, reconciliation of comments, document finalisation and approval.

The Medical Writer works towards the timely development of these documents in agreement with deadlines set together with the Study Team, the Medical Director and the Regulatory Affairs Department.

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