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 We’re 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. You’ll work with cutting-edge technologies and have a meaningful impact on advancing healthcare.

To apply:

nfordyce@barringtonjames.com

+44 1293 243 844

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