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About Our Medical Writer Contract Roles
What does a medical writer contractor do?
Organisations bring in Medical Writer contractors to produce the clear, accurate, and scientifically rigorous written materials that support drug development, regulatory submissions, publication of clinical research, and medical education within the pharmaceutical, biotechnology, and medical device industries. The scope of medical writing contracting is broad: regulatory medical writers develop the clinical study reports, investigator brochures, summary of product characteristics, and briefing documents required for marketing authorisation submissions; publication writers prepare manuscripts, abstracts, and conference presentations from clinical trial data for peer-reviewed journals and congresses; medical communications writers develop educational materials, advisory board content, and disease awareness programmes. The common thread is the need to translate complex scientific and clinical data into accurate, well-structured written content appropriate for its specific regulatory or scientific audience.
Medical Writer contractors are expected to combine scientific or clinical training with exceptional writing skills and deep familiarity with the specific documentation types they produce. A degree in a life sciences discipline is expected as a baseline, with a postgraduate qualification or industry experience providing the scientific depth needed to write about complex therapeutic areas credibly. For regulatory medical writers, thorough knowledge of ICH guidelines, particularly E3 for clinical study reports and M4E for CTD electronic submissions, is essential. Proficiency in the relevant regulatory submission formats and familiarity with regulatory agency expectations is expected for senior regulatory writing roles. Medical writing qualifications from AMWA or EMWA are well regarded and signal professional commitment to the discipline.
What is the market like for medical writer contractors?
The Medical Writer contract market is a specialist and consistently active market within the life sciences sector, driven by the ongoing pipeline of clinical drug development, regulatory submissions, and scientific publications generated by pharmaceutical and biotech companies. The concentration of pharmaceutical and biotech activity in the UK, combined with the global reach of clinical development programmes run from UK-based medical affairs and regulatory functions, ensures a consistent demand for experienced medical writers. Regulatory medical writers, particularly those with experience writing CTD-format submissions for EMA or MHRA, are among the most in-demand and highest-paid specialists within the medical writing contractor market.
How much do medical writer contractors usually earn?
Contract rates for medical writer roles typically range from £400 to £750 per day, depending on the scope of the role, required expertise, and the delivery expectations of the engagement.
How many medical writer vacancies are there on Quality Contracts?
Over the past twelve months, we have tracked over 100 medical writer contract roles across the site. Data reviewed up to June 2026.