Requirements: English
Company: Barrington James
Region: Dijon , Bourgogne-Franche-Comt
Barrington James is seeking a Clinical Affairs Officer to join an innovative and fast-growing medical device organisation. This role offers the opportunity to take ownership of clinical and regulatory activities, making a real impact in the healthcare industry!Key Responsibilities:Conduct scientific and competitive intelligence , including literature reviews, analysis of competitor products, and maintaining a bibliographic repository.Develop and manage clinical safety documents , such as Clinical Evaluation Reports (CER) and Post-Market Clinical Follow-up (PMCF) studies.Take ownership of clinical studies by designing protocols, managing collaborations with CROs, and analysing results.Support the regulatory affairs team with product registrations and drafting essential clinical reports.What Were Looking For:A biomedical engineering or health/biomedical graduate with at least 2 years of experience in clinical and regulatory affairs for medical devices.Expertise in drafting key documents (CER, PMCF, PSUR) and knowledge of medical device regulations (MDD/MDR, ISO 14971, ISO 13485).Strong bibliographic research and analytical skills, with professional-level English writing ability.A self-motivated, detail-oriented individual with a curious mindset and excellent communication skills.This is a unique opportunity to take full ownership of clinical and regulatory functions within a forward-thinking organisation. Youll work with cutting-edge technologies and have a meaningful impact on advancing healthcare.To apply:nfordyce@barringtonjames.com+44 1293 243 844