Associate Director, Medical Advisor (Oncology)

The Associate Director, Senior Medical Advisor assists in the development of medical strategy, planning, and execution of oncology-related medical affairs activities at Regeneron UK.

This hire provides scientific and/or medical expertise by thoroughly understanding oncology, particularly immuno-oncology, and serves as a scientific/medical resource. The Associate Director will work in a multifunctional, matrix organization, closely collaborating with colleagues within the medical affairs group (including field medical, medical operations, medical education, global medical communications, and HEOR) as well as with those in research & development, commercial, access & reimbursement, and patient advocacy. Actively participates in and contributes to the cross-functional Medical Product Team.

A typical day may include the following:

• Serving as the local Regeneron medical contact in country for assigned Oncology asset and pipeline. This person is a key contact for both local internal (clinical development, medical affairs, operations, regulatory, commercial) and external (medical societies, key academic and medical experts) collaborators.
• Maintaining deep scientific and medical Oncology knowledge, particularly in the lung cancer field, and an understanding of patient and physician interactions and clinical decision making and impact.
• Being the key medical contact for the review of all promotional and non-promotional materials developed by the oncology brand team.
• Identifying and contributing to data analyses, data interpretation, and publication development in collaboration with the publications lead and biostatistics. Compliantly engaging external and internal authors during the development of congress presentations and manuscripts and during internal review processes, working closely with the Publication Manager.
• Contributing to the development and management of appropriate medical affairs research programs, including collaborative studies, expanded access programs, and company-sponsored studies.
• Participating in scientific engagement with external communities to educate and advance scientific and medical understanding of oncological and/or haematological diseases, the management of disease, standards of patient care, and roles of our medicines.
• Helping to develop medical content for congresses, symposia, and advisory boards and leading or participating in such activities.
• Presenting scientific/medical materials to diverse audiences (e.g., physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in meetings, including payer, advisory, and/or consulting settings.
• Assessing medical education needs and working with Medical Education colleagues to review internal and external educational activities. Assisting in medical monitoring of post-registrational trials and in the review of documents related to the interpretation of patient-level data where necessary.

This role may be for you if:

• You enjoy working hard; are willing to take action and are full of energy for the things you see as challenging.
• You have a commitment to become an ABPI final medical signatory.
• You have the ability to engage in collaborative decision-making to complete tasks in a timely fashion and function in a fast-paced and rapidly expanding environment. You are a practical problem solver, identifying simple, realizable solutions.
• You can prioritize and manage multiple projects/activities and perform well under pressure; able to maintain composure in challenging situations.
• You possess the ability to engage in positive dialogues, influence outcomes, and resolve conflicts in a constructive manner.

We are seeking healthcare professionals (ideally a registered GMC MD or a registered pharmacist) possessing some prior Oncology therapeutic experience in solid tumors. 3+ years of relevant experience in the pharmaceutical industry, disease management programs, or clinical pharmacy/medicine. Demonstrates strong written, interpersonal, and excellent verbal communication skills. We need an individual with strategic agility and the ability to work with multiple collaborators. Outstanding work ethic and integrity, including high ethical and scientific standards. Strong interpersonal skills particularly motivational, negotiation, listening, judgment, analytic, and conflict management skills. Level commensurate with years of experience.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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!

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.

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.

Please note that certain background checks will form part of the recruitment process. 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.