Medical Writer (m/w/d)
Core
Draft, edit, and manage clinical regulatory documents (CERs, CEPs, PMCF plans/reports) and scientific articles for aortic disease medical devices.
Role type
Medical Writer (Clinical Regulatory)
Builds
Clinical evaluation reports, clinical evaluation plans, post-market clinical follow-up plans, and scientific articles
Domain
Medical Devices / Cardiovascular
Required skills
Medical writing, regulatory writing, clinical knowledge, medical literature research, data analysis, content development, document management, cross-functional collaboration
Preferred skills
EU MDR experience, experience with CERs/CEPs/PMCF, Cardiovascular background, PhD or MD
Technologies
None stated
Responsibilities
Draft, edit, and proofread clinical documents; Conduct literature searches and appraisals; Coordinate document timelines; Collaborate with Clinical, R&D, and Regulatory teams; Support meetings related to clinical content
Seniority
Mid-level (3–4 years experience)