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Your New Company
A global biotechnology company is seeking a visionary Regulatory Affairs Senior Manager to drive their expanding oncology portfolio from a strategic perspective. 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
I am looking for a strategic thinker with proven experience developing and implementing regulatory strategies for clinical-stage products in the EU and US (Benefit). Experience with Scientific Advice, PIPs, and ODDs will help you hit the ground running.
Location & BenefitsThis 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.
