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    <title>Senior Medical Writer - Talentmark RSS Feed</title>
    <link>https://jobs.co.uk/job/senior-medical-writer-talentmark--21312409-a665-4899-914c-64ff029104e5</link>
    <description>RSS feed for Senior Medical Writer at Talentmark.</description>
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    <lastBuildDate>Fri, 10 Jul 2026 20:10:20 GMT</lastBuildDate>
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      <title>Senior Medical Writer - Talentmark</title>
      <link>https://jobs.co.uk/job/senior-medical-writer-talentmark--21312409-a665-4899-914c-64ff029104e5</link>
      <guid>https://jobs.co.uk/job/senior-medical-writer-talentmark--21312409-a665-4899-914c-64ff029104e5</guid>
      <pubDate>Thu, 09 Jul 2026 23:00:00 GMT</pubDate>
      <description>Location: Welwyn Garden City | Salary: &amp;pound;60 - &amp;pound;75/hour | Type: Contract | Talentmark are recruiting for a  Senior Medical Writer  to join a company in the pharmaceutical industry on a contract basis for  12 months .    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.   Your Background:     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 c...</description>
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