Senior Medical Writer (Remote - UK)
Remote · London, England, United Kingdom or GB
Job Summary
Senior Medical Writer (Remote - UK) at MMS, a CRO, responsible for writing and editing clinical development documents (protocols, investigator’s brochures, clinical study reports, informed consent forms, safety summaries) and related materials; manage timelines, mentor other writers, and coordinate with clients to ensure regulatory standards and templates are followed. Requires 3+ years in pharma, 3-5 years regulatory/clinical medical writing, and advanced MS Word/office suite skills; ideal candidate holds a Bachelor, Master, or PhD in a scientific/medical discipline with experience leading teams and regulatory submissions. Remote role based in the UK (London area) with no specified relocation requirement beyond standard expectations.
Required Qualifications
- 3+ years in pharmaceutical industry
- 3-5 years regulatory writing and clinical medical writing experience
- Bachelor/Master/PhD in scientific/medical field
- experience leading teams
- experience with regulatory submissions
- experience with clinical data
Additional Requirements
- None specified
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