Overview

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).

A MedTech company is seeking a Medical Writer with proven medical device experience to support their expanding clinical research portfolio. With Class II devices already sold globally, they are diversifying their products and running a wide range of new clinical trials.

The role

You’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 teams

What you need to bring

• 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 frameworks

Please note: Candidates must already be based in the UK with the right to work. Sponsorship or post-study visas with restrictions cannot be considered.

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 Josh@Indoprofessionals.co.uk to discuss.

Job details

• Seniority level: Associate
• Employment type: Full-time
• Job function: Writing/Editing, Research, and Science
• Industries: Medical Equipment Manufacturing

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