Senior Manager Regulatory Affairs EU Oncology

hays-gcj-v4-pd-online; London; Hybrid; GBP 75,000 - 100,000; Full time

Job summary

A global biotechnology company is seeking a Senior Manager Regulatory Affairs for oncology in London. This role involves driving regulatory strategies for clinical-stage oncology products, navigating complex approval pathways, and collaborating with health authorities. The position offers hybrid work with potential for extension.

Qualifications

• Proven experience in regulatory affairs for clinical-stage products in the EU and US.
• Experience with Scientific Advice, PIPs, and ODDs preferred.

Responsibilities

• Lead development and execution of regulatory strategies for clinical-stage oncology products.
• Guide products through critical regulatory milestones.
• Foster relationships with health authorities.

Skills

Strategic Thinking

Regulatory Strategy Development

Collaboration

Relationship Building

Job description

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Senior Manager Regulatory Affairs EU Oncology, London

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Client:

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

3962050ba07b

Job Views:

35

Posted:

22.06.2025

Expiry Date:

06.08.2025

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Job Description:

Your 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. 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. #4687831 - Julia Bowden