Senior Medical Writer
Talentmark
Remote-friendly
Salary:
£45.50 to £56.40 per hour PAYE or £60 to £75 per hour Umbrella/Limited.
Senior Medical Writer Role:
- Lead a team of Content Strategists and cross-functional colleagues to build content strategy for global regulatory submissions.
- Plan timelines for producing and reviewing documents, keeping them aligned with wider project deadlines.
- Review documents for clarity, structure, and scientific accuracy.
- Act as a key voice in functional and cross-functional teams, helping shape best practice and drive improvements.
- Keep your knowledge sharp on regulatory, scientific, and medical developments relevant to the therapeutic area.
- Degree in Life Sciences or equivalent, with at least 5 years' experience in pharma or biotech.
- Solid understanding of global drug and device development processes and regulations, including GxP, GCP, ICH, ISO, and MDR/IVDR.
- Strong background in clinical, safety, or device regulatory documentation across the full product lifecycle.
- Able to independently analyse and pull together clinical and non-clinical data from a range of disciplines.
- Skilled in G Suite, Microsoft Office, Adobe Acrobat, and Veeva Vault.
Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products.
Location:
This role offers hybrid or fully remote working with our client.
Apply :
For more information, or to apply for this Senior Medical Writer role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference 194 284.
It is essential that applicants hold entitlement to work in the UK.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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