<?xml version="1.0" encoding="utf-8"?>
<rss version="2.0">
  <channel>
    <title>Regulatory Medical Writer - IND, CTA, NDA, MAA, BLA - Hays Life Sciences RSS Feed</title>
    <link>https://jobs.co.uk/job/regulatory-medical-writer-ind-cta-nda-maa-bla-hays-life-sciences--ab78a41a-061b-4e63-8fc7-f2724853db6a</link>
    <description>RSS feed for Regulatory Medical Writer - IND, CTA, NDA, MAA, BLA at Hays Life Sciences.</description>
    <language>en-gb</language>
    <lastBuildDate>Thu, 11 Jun 2026 01:07:59 GMT</lastBuildDate>
    <item>
      <title>Regulatory Medical Writer - IND, CTA, NDA, MAA, BLA - Hays Life Sciences</title>
      <link>https://jobs.co.uk/job/regulatory-medical-writer-ind-cta-nda-maa-bla-hays-life-sciences--ab78a41a-061b-4e63-8fc7-f2724853db6a</link>
      <guid>https://jobs.co.uk/job/regulatory-medical-writer-ind-cta-nda-maa-bla-hays-life-sciences--ab78a41a-061b-4e63-8fc7-f2724853db6a</guid>
      <pubDate>Sun, 07 Jun 2026 23:00:00 GMT</pubDate>
      <description>Location: Welwyn Garden City | Salary: &amp;pound;70.00 - &amp;pound;90.00/hour &amp;pound;70 - &amp;pound;90 p/h OUTSIDE IR35 | Type: Contract | Your new company   My client, a global biopharmaceutical company with a goal of contributing to healthcare innovation and environmental sustainability and which is focused on improving people''s quality of life, specialising in Oncology, neurology and rare diseases, and has a position available for a Regulatory Medical Writer to join their Non-clinical Submission &amp; Documentation Management team on an initial 12-month contract.   Remote  12 Month + Contract  Outside IR35  -75 p/h - -90 p/h   Your new role   As the Regulatory Documentation Scientist (non-clinical scientific writer), you will manage the submission of authored non-clinical documents to regulatory agencies in support of applications such as INDs, CTAs, NDAs, MAAs, and BLAs. With your scientific writing capabilities, you will ensure that the documents are clearly written, accurate and consistent, adhere to the company''s and ICH standards, and that they are reviewed and approved by the appropriate functional groups.   Manage the preparation, review, and submission of non-clinical summary documents for both early development and marketing applications  Work with regulatory and scientific functions to ensure comprehensive ...</description>
      <category>Contract</category>
    </item>
  </channel>
</rss>