Recruiter listing several UK medical affairs medical writing roles at agencies, from mid-level to principal, covering scientific content and medical education.
Medical writing roles
Full-time and part-time roles at pharma, biotech, CROs and medcomms agencies.
148 roles · 148 new this week
Senior medical science writer producing publications, literature reviews and scientific content on neuromodulation therapies for healthcare professionals.
Part-time remote role drafting and leading manuscripts, grant applications and technical reports for health systems and population science researchers.
SEO content writing for a UK medical cannabis clinic, producing accurate, compliant health articles, web pages and patient stories for patients.
Regulatory medical writer creating clinical documents for drug submissions, such as clinical overviews and briefing documents, for pharma project teams.
Remote senior medical writing role at Stryker's Neurovascular Division, leading clinical evidence strategy and regulatory documents for medical devices.
Remote medical writing role focused on abstracts, posters and manuscripts for a publications-led life sciences client team.
SEO-focused web copywriting for medical practices, hospitals and healthcare providers, including site pages, blogs and promotional content, at a web agency.
Writing clinical and regulatory documents for oncology trials, such as protocols, CSRs and IND or NDA sections, for a growing life sciences company.
Remote medical writing role preparing regulatory-compliant clinical trial documents, regulatory submissions and publications for life sciences clients.
Remote senior regulatory medical writing role preparing CSRs, IBs and CTD modules for a global pharmaceutical company, via a recruiter.
Associate director leading clinical regulatory document development across global programs and mentoring writers at a biopharma company.
Writes promotional copy for pharmaceutical brands across media, working with art directors and cross-functional teams at a healthcare agency in Toronto.
Writes and revises print and digital pharmaceutical copy, including FDA-compliant and SEO content, for clients of a global professional services firm in Toronto.
Senior analyst delivering HTA submissions, value materials and health economic models for medcomms clients, with scientific writing and project ownership.
Leads publication projects and scientific writing at a Boston medical communications agency, overseeing quality, timelines and mentoring colleagues.
Scientist role designing genetic medicine case studies and reviewing AI agent outputs for scientific soundness, for AI benchmark work.
Manages a team of medical writers preparing clinical documents for immunology programmes at a large pharmaceutical company.
Manager role leading EMEA medical information content and healthcare professional responses for a biopharma developing neuromuscular disease treatments.
Authoring clinical study reports, protocols and regulatory submission documents, with client coordination, for a biopharma development partner.