Director, Medical Affairs Lead Haematology

Regeneron Pharmaceuticals; Greater London; On-site; GBP 200,000 +; Full time

Job summary

A leading biotech firm in the UK is looking for a Medical Affairs Lead in haem-oncology. The role involves overseeing the medical strategy for multiple myeloma and lymphoma while collaborating with various internal teams. Ideal candidates will have an M.D. or PhD and experience in pharmaceutical Medical Affairs, with a strong knowledge of relevant codes. This position requires excellent leadership and communication skills while engaging with key stakeholders in the field.

Benefits

Health and wellness programs

Fitness centers

Equity awards

Annual bonuses

Paid time off

Qualifications

• Expertise in haem-oncology with experience in Medical Affairs.
• Strong knowledge of ABPI and IPHA codes.
• Ability to build relationships with key stakeholders.
• Proven leadership and strong communication skills.

Responsibilities

• Serve as the in-country medical contact for haem-oncology.
• Collaborate with internal teams for strategic planning.
• Manage and develop a high-performing medical team.
• Provide medical support for clinical development activities.
• Stay updated on scientific advancements in haem-oncology.
• Lead medical education initiatives aligned with local needs.

Skills

EMR Systems

Clinical Research

Leadership Experience

Clinical Development

Managed Care

Primary Care Experience

Education

M.D. or PhD in haem-oncology

Job description

Overview

Are you ready to make a meaningful impact in the field of haem‑oncology? At Regeneron we are seeking a dedicated Medical Affairs Lead to be the driving force behind our haem‑oncology program in multiple myeloma and lymphoma. As a pivotal member of our team you will serve as the medical contact in‑country, collaborating with internal teams and external stakeholders to advance scientific understanding, improve patient care and ensure the success of our therapeutic strategies. Join us in shaping the future of haem‑oncology while working in a dynamic and supportive environment.

Typical Day

• Represent Regeneron as the in‑country medical contact for haem‑oncology, engaging with medical societies, academic leaders and thought leaders.
• Collaborate with cross‑functional teams including clinical development, regulatory, market access and commercial colleagues to optimise strategic and tactical planning.
• Manage and develop a high‑performing haem‑oncology medical team, ensuring compliance, training, coaching and execution of initiatives.
• Provide medical support for clinical development activities such as identifying key investigators and supporting patient recruitment efforts.
• Stay updated on scientific advancements and therapeutic developments in haem‑oncology to enhance strategic decision‑making.
• Participate in scientific engagements and deliver impactful presentations to diverse audiences, including healthcare professionals and stakeholders.
• Lead medical education initiatives, ensuring alignment with local needs and compliance with ABPI and IPHA codes.
• Collaborate with global teams to prepare for product launches, market access strategies and life‑cycle management initiatives.

This Role May Be For You If You:

• Are a physician (M.D.) or scientist (PhD) with expertise in haem‑oncology and experience in Medical Affairs within the pharmaceutical or biotech industry.
• Have a strong knowledge of ABPI and IPHA codes coupled with experience supporting research and clinical development in the UK.
• Excel at building relationships with key stakeholders, including thought leaders, and can cultivate trust through scientific expertise and follow‑through.
• Possess strong leadership skills, inspiring and motivating teams while fostering collaboration and inclusion.
• Are proactive, resourceful and thrive in a fast‑paced, innovative environment.
• Are skilled at juggling multiple projects, delivering actionable insights and maintaining attention to detail.
• Embody an entrepreneurial attitude and demonstrate a commitment to ethical and scientific standards.
• Are fluent in English and willing to travel 30–50% of the time.

To Be Considered

Applicants must hold an M.D. or PhD with expertise in haem‑oncology and have substantial pharmaceutical or biotech industry experience in Medical Affairs. A thorough understanding of the UK healthcare environment and ABPI / IPHA codes is essential. Preferred candidates will have experience supporting clinical development in haem‑oncology, a solid background in life‑cycle product development and a proven ability to work cross‑functionally in matrix environments. Strong leadership, communication and organisational skills are critical for success in this role.

Key Skills

• EMR Systems
• Post Residency Experience
• Occupational Health Experience
• Clinical Research
• Managed Care
• Primary Care Experience
• Medical Management
• Utilisation Management
• Clinical Development
• Clinical Trials
• Leadership Experience
• Medicare

Employment Type

Full‑Time

Experience

years

Vacancy

1

Background Checks

Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications, etc.

Benefits

Join Regeneron and contribute to advancing haem‑oncology care while working with a team of passionate professionals dedicated to innovation and patient outcomes. Apply today to make a difference! We have an inclusive and diverse culture that provides comprehensive benefits which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses and paid time off for eligible employees at all levels.

Equal Opportunity Statement

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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment unless the accommodation would impose undue hardship on the operation of the Company’s business.

Salary Information

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles that will be based in Japan and / or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S., Japan or Canada, please speak with your recruiter about salaries and benefits in your location.