Senior Manager Regulatory Affairs EU Oncology

TN United Kingdom; London; Hybrid; GBP 70,000 - 90,000; Full time

Job summary

A leading global biotechnology firm is seeking a Senior Manager for Regulatory Affairs in Oncology. This role involves crafting regulatory strategies for clinical-stage oncology products and fostering relationships with health authorities. The position offers hybrid work and a chance to impact cancer treatment delivery across EU markets.

Benefits

Hybrid Work

Monthly Team Meetings

Qualifications

• Proven experience developing regulatory strategies for clinical-stage products in EU and US.
• Experience with Scientific Advice, Pediatric Investigation Plans, and Orphan Drug Designations is advantageous.

Responsibilities

• Lead development and execution of regulatory strategies for oncology products.
• Guide products through regulatory milestones from early development to market approval.
• Provide strategic regulatory guidance to cross-functional teams.

Skills

Strategic Thinking

Regulatory Strategy Development

Collaboration

Job description

Senior Manager Regulatory Affairs EU Oncology, London

Client: [Client details not provided]

Location: London, United Kingdom

Job Category: Other

Job Type: Virtual job fairs

EU work permit required: Yes

Job Reference: 3962050ba07b

Job Views: 3

Posted: 17.05.2025

Expiry Date: 01.07.2025

Job Description:

Your company, a global biotechnology firm, is seeking a visionary Regulatory Affairs Senior Manager to lead 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. Your responsibilities include crafting regulatory strategies to navigate complex approval pathways and building relationships with health authorities.

Your Expertise & Impact

• Lead development and execution of regulatory strategies for clinical-stage oncology products
• Lead EU Clinical Trial Regulation (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 candidates are strategic thinkers with proven experience developing and implementing regulatory strategies for clinical-stage products in the EU and US. Experience with Scientific Advice, Pediatric Investigation Plans (PIPs), and Orphan Drug Designations (ODDs) is advantageous.

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.

To apply, submit your CV or contact Julia Bowden to discuss this opportunity further. #4687831 - Julia Bowden

Please note: If you are not a passport holder of the country for the vacancy, you might need a work permit. For more information, check our Blog.

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Created on 17/05/2025 by TN United Kingdom