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    <title>Regulatory Affairs Manager Oncology CTA - Hays Life Sciences RSS Feed</title>
    <link>https://jobs.co.uk/job/regulatory-affairs-manager-oncology-cta-hays-life-sciences--b694c5cb-6287-4253-bd30-963b924bd6e7</link>
    <description>RSS feed for Regulatory Affairs Manager Oncology CTA at Hays Life Sciences.</description>
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    <lastBuildDate>Thu, 23 Jul 2026 21:20:53 GMT</lastBuildDate>
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      <title>Regulatory Affairs Manager Oncology CTA - Hays Life Sciences</title>
      <link>https://jobs.co.uk/job/regulatory-affairs-manager-oncology-cta-hays-life-sciences--b694c5cb-6287-4253-bd30-963b924bd6e7</link>
      <guid>https://jobs.co.uk/job/regulatory-affairs-manager-oncology-cta-hays-life-sciences--b694c5cb-6287-4253-bd30-963b924bd6e7</guid>
      <pubDate>Tue, 21 Jul 2026 23:00:00 GMT</pubDate>
      <description>Location: Cambridge | Salary: &amp;pound;450 - &amp;pound;490/day Competitive Rate | Type: Contract | An exciting opportunity has arisen for an experienced Regulatory Affairs Manager to support innovative oncology and advanced therapy programmes within a global biopharmaceutical environment.   This role will play a key part in driving regulatory strategy, leading Clinical Trial Applications (CTA), EU CTR submissions, substantial amendments, and broader regulatory activities across EU. Working closely with global and regional stakeholders, you will support the development of cutting-edge therapies in a fast-paced, highly collaborative setting. Key Responsibilities   Lead regulatory affairs activities for development-stage and marketed products.  Drive CTA submissions, amendments and EU CTR activities across Europe.  Develop and execute regulatory strategy in partnership with global regulatory teams.  Prepare and coordinate regulatory submissions in line with EU and ICH requirements.  Represent Regulatory Affairs within cross-functional project teams.  Monitor evolving European regulatory requirements and provide strategic guidance to stakeholders.    Experience Required   Proven experience within Regulatory Affairs in the pharmaceutical or biotech sector.  Strong knowledge of Clinic...</description>
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