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About the Role
Provide scientific and medical leadership across our oncology portfolio and pipeline. Serve as a trusted medical expert, partnering with internal stakeholders and external healthcare professionals to shape medical strategy, support launches, and advance scientific exchange across the UK.
Responsibilities
- Serve as the UK medical lead for assigned oncology assets and pipeline products.
- Build and maintain scientific relationships with healthcare professionals, key opinion leaders, scientific societies, and other external stakeholders.
- Partner cross-functionally with Clinical Development, Commercial, Regulatory, Market Access, and Global Medical Affairs teams.
- Provide scientific and medical input into product strategy, launch readiness, lifecycle management, and evidence-generation activities.
- Support advisory boards, scientific meetings, congresses, and educational initiatives.
- Deliver high-quality scientific presentations and communicate complex medical information to diverse audiences.
- Contribute to clinical development activities through engagement with investigators, research centers, and oncology networks.
- Review and approve materials in accordance with the UK ABPI Code of Practice.
- Identify unmet medical needs and generate insights to inform medical strategy.
- Ensure all activities are conducted in compliance with applicable regulations and company policies.
Requirements
- Advanced scientific degree (MD, PharmD, PhD, MSc or equivalent) in Medicine, Pharmacy, Life Sciences, or a related discipline.
- Significant Medical Affairs experience within the pharmaceutical or biotechnology industry, including substantial Oncology experience.
- Strong knowledge of Medical Affairs and Clinical Development within the UK healthcare environment.
- Experience engaging and collaborating with Key Opinion Leaders and other external experts.
- Working knowledge and experience reviewing materials in accordance with the UK ABPI Code.
- Experience working successfully within a matrix, cross-functional organization.
- Excellent scientific communication and stakeholder engagement skills.
- Ability to build and maintain trusted relationships with internal and external stakeholders.
- Strong strategic thinking, analytical, and problem-solving capabilities.
- Ability to manage multiple priorities in a fast-paced environment.
- A proactive, self-directed, and entrepreneurial approach.
- Strong commitment to compliance, ethics, and scientific integrity.
- Fluency in English.
- Ability and willingness to travel 20-30%, including international travel.
Skills
- GMC-registered physician or registered pharmacist (preferred).
- Final Medical Signatory certification or interest in becoming a Final Medical Signatory for the UK and Ireland (preferred).
- Previous clinical practice experience (preferred).
- Product launch experience within Oncology (preferred).
- Experience in Skin Cancer, Immuno-Oncology, and/or Solid Tumours (preferred).
- Existing relationships within the UK oncology community (preferred).
- Strong leadership, influencing, negotiation, and collaboration skills (preferred).
Location
- Uxbridge, UK
Work Type
- Hybrid working model
Experience Level
- Associate Director
Education Level
- Advanced scientific degree (MD, PharmD, PhD, MSc or equivalent) in Medicine, Pharmacy, Life Sciences, or a related discipline.
Benefits
- Annual bonuses or other incentive plans.
- Equity awards.
- Pension or retirement benefits.
- 401(k) company match.
- Health and wellness programs.
- Fitness centers.
- Insurance benefits (e.g. medical, dental, vision, life and disability).
- Paid time off.
- Family support benefits.
About the Company
- At Regeneron, our Medical Affairs professionals play a critical role in advancing scientific understanding, supporting evidence generation, and improving outcomes for patients living with cancer.
Equal Opportunity
- Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.
- Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.