Job Title

Medical Writer (Clinical Trials) Medical Devices Remote with occasional travel required (South Wales / London)Must already be UK-based with full right to work (post-study work visa cannot be considered) Have you written Clinical Evaluation Reports (CERs) that shaped a clinical trial in medical devices?This growing MedTech company is looking for a Medical Writer with proven medical device experience to support their expanding clinical research portfolio. With Class II devices already sold globally, they are now diversifying their products and running a wide range of new clinical trials — making this a great time to join.The roleYou’ll work independently to:• Draft and update Clinical Evaluation Reports (CERs), Clinical Investigation Plans (CIPs), Final Study Reports (FSRs), and participant-facing documents• Translate data into regulatory submissions, publications, and posters• Ensure compliance with ISO 14155, EU MDR, FDA regulations, and ICH-GCP• Collaborate with clinical, regulatory, and biostats teamsWhat you need to bring• A Life Sciences degree (postgraduate preferred)• Ideally 3–5 years’ medical writing experience in MedTech clinical trials• Strong track record of CER authorship and clinical trial documentation• The ability to work independently without heavy oversight• Solid understanding of ISO 14155, GCP, EU MDR, and FDA frameworksPlease note: Candidates must already be based in the UK with the right to work. Unfortunately, sponsorship or post-study visas with restrictions cannot be considered.Why join?You’ll be part of a company that genuinely values evidence, not marketing fluff. Their products are award-winning, clinically validated, and in demand worldwide. With everything from R&D to regulatory in-house, you’ll be close to the action — and part of a clinical team that is growing fast.Apply today or contact to discuss.