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 & 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.