Medical Director, Medical Affairs – Dermatology in Sleepy Hollow, NY | Regeneron Careers | Apply Now!
Are you a visionary medical leader with a passion for Dermatology and a track record in Medical Affairs? Regeneron is seeking a Medical Director to shape and execute medical strategy for our Dermatology pipeline, based at our Sleepy Hollow, NY campus. As a global biotechnology leader, Regeneron is driven by science and committed to patient-focused innovation. In this pivotal role, you’ll lead initiatives across clinical research, scientific communications, and strategic collaborations — helping us set new standards in dermatological care.
About the Company: Regeneron
At Regeneron, we use the power of science to bring new medicines to patients who need them most. Founded in 1988 and headquartered in Tarrytown, New York, we are a fully integrated biotechnology company that invents, develops, and commercializes life-transforming medicines. Our breakthroughs in genetics, antibody technology, and disease biology have made us a global leader in areas such as immunology, oncology, ophthalmology, and dermatology. Our mission is driven by curiosity, excellence, and a deep commitment to scientific truth and patient care. At Regeneron, you’ll find a culture built on innovation, collaboration, and the highest ethical standards — where every team member has the opportunity to contribute to something bigger than themselves. We’re not just developing treatments. We’re redefining what’s possible in science and medicine.
Job Details:
Job Posting: Medical Director, Medical Affairs-Dermatology
Location: Sleepy Hollow, New York, United States of America
Department: Global Development
Job Req ID: R34898
Job Description:
As a Medical Director, you will help lead the development of our Dermatology medical strategy, planning & execution our of medical affairs activities with the patient at the forefront ensuring activities are delivered with integrity and scientific accuracy.
Location:
This position will require you to be on-site for 4 days/week at our Sleepy Hollow, NY location and 1 day/week work from home. We are not able to accommodate a fully remote option. If eligible, we can offer relocation benefits.
Responsibilities:
- Developing and leads all aspects of implementation of medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations within the healthcare community.
- Applying therapeutic/disease area expertise and business understanding to address current and future medical needs in clinical practice with medically appropriate use of investigational medicines.
- Overseeing and provides hands on support in management, generation and dissemination of clinical and non-clinical data and results in high quality publications.
- Acting as standing or ad-hoc member for various teams; provides scientific/medical perspectives to the global and US strategic and medical organizations.
- Co-leads the formation, refinement and execution of a robust Phase 3b/4 plan
Supporting the design, conduct, oversight, analysis and reporting of Medical Affairs clinical trials. Ensures timely submission and delivery of high-quality clinical trial documentation, implementation and execution. - Continuing to develop and cultivate long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external collaborators representing.
- Prioritizing support of investigator-initiated studies and serves as a key member of internal Scientific Review Committees.
- Ensuring accuracy of training material for scientific and product information.
- Coordinating medical review and approval of promotional materials.
- Ensuring goals and objectives are met and projects completed on time and within budget.
- Is responsible for optimal medical affairs resource allocation across the spectrum of a product’s life cycle.
- Oversees development and forecasting of project budgets across assets.
- Champions high standards of compliance, ethics and patient safety, putting patients at the center of all actions.
- Performs medical monitoring of post-registrational trials and is the signatory of documents related to interpretation of patient level data where necessary.
- Interacts internally and externally with senior management and functional heads.
- Represents Medical Affairs on the Strategic Product Team.
- Works in a goal/objective oriented manner within formalized process to plan and implement annual goals in alignment with the corporate annual goals and core business strategy.
- Potential to supervise Medical Directors and/or Associate Director.
This may be for you:
- Want to challenge the standard of patient care
- Are at ease with an abundance of detail and complexity. Deals with scientific concepts and complexity with confidence.
- Makes the best decision possible based on a mixture of data analysis, wisdom, experience and judgment.
- Outstanding work ethic and integrity, including high ethical and scientific standards
Requirements:
- To be considered it is essential to have a Medical (MD / MBBS or equivalent) including >7 years of medical affairs or clinical development experience. Solid background and experience in drug development and life-cycle development of immunology related products required. Dermatology experience is required. Any alliance related setting experience is preferred.
- Additional requirements include:
- Demonstrated experience leading technical and business discussions internally and externally and explain scientific/medical concepts to all levels.
- Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields.
- Ability to establish trust through the consistent demonstration of scientific expertise and follow-through on requests from key opinion leaders
- Strong leadership and management skills.
Salary Range: $275,200.00 – $372,400.00
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