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Regulatory Affairs Senior Manager contract EU Oncology

Hays Specialist Recruitment Limited
Posted 15 days ago, valid for 24 days
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Salary

£60,000 - £72,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Global Biotechnology is seeking a Regulatory Affairs Senior Manager to lead their oncology portfolio across Europe.
  • The role involves crafting regulatory strategies, guiding products through milestones, and building relationships with health authorities.
  • Candidates should have a proven background in developing regulatory strategies for clinical-stage products, with experience in Scientific Advice, PIPs, and ODDs.
  • This position is a 12-month contract with a salary of £80,000 to £90,000 and requires at least 5 years of relevant experience.
  • The role offers hybrid work with monthly team meetings in Uxbridge/Cambridge, emphasizing innovation and collaboration.

Help Shape the Future of Cancer Treatment

Are you passionate about bringing innovative oncology treatments to patients across Europe? Global Biotechnology, a leading UK-based company, is seeking a visionary Regulatory Affairs Senior Manager to drive their expanding oncology portfolio.Shape Global Strategy & Patient Impact Join this dynamic Global Regulatory Team where you'll play a pivotal role in bringing life-changing cancer treatments from development to patient delivery across EU markets. You'll craft regulatory strategies that navigate complex approval pathways and build crucial relationships with health authorities.

Your Expertise & Impact

  • Lead development and execution of regulatory strategies for clinical-stage oncology products
  • Lead EU CTR Submission strategies
  • Guide products through critical regulatory milestones from early development to market approval
  • Foster collaborative relationships with health authorities
  • Provide strategic regulatory guidance to cross-functional teams

Ideal Background I am looking for a strategic thinker with proven experience developing and implementing regulatory strategies for clinical-stage products. Experience with Scientific Advice, PIPs, and ODDs will help you hit the ground running.

Location & Benefits This 12-month contract (with potential extension) offers hybrid work with monthly team meetings in Uxbridge/Cambridge. Join a company that values innovation, collaboration, and making a real difference in patients' lives.Apply now by submitting your CV, or reach out to Julia Bowden to discuss this opportunity further.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.