About

We are seeking an experienced medical writer to support the development of Clinical Evaluation Reports (CERs) in compliance with EU MDR requirements for Class III medical devices. The ideal candidate will have a proven track record of preparing CERs and related documentation under MDR/MEDDEV and experience in writing Clinical Evaluation Plans, Literature Review Protocols, and Reports. The candidate should be able to synthesize data from published literature, clinical studies, and post-market sources, ensuring all deliverables meet MDR, MEDDEV 2.7/1 rev. 4, and MDCG guidance requirements.