Senior Director, Medical Affairs, Ophthalmology (EYLEA)

Tarrytown, NY, United States
Nov 15, 2020
Required Education
Position Type
Full time
The Senior Director of Medical Affairs provides strategic leadership with high visibility in the organization, reporting into the Executive Director of Medical Affairs. She/he orchestrates the development of medical strategy, planning and execution of medical affairs activities at Regeneron with the benefit of the patient at the forefront. He/she will provide leadership by thoroughly understanding ophthalmology and serving as a scientific and medical resource.
The Senior Director will lead a multifunctional Medical Product Team (MPT) within a matrix organization, consisting of colleagues within the medical affairs group. The Senior Director ensures alignment working closely with research & development, commercial, access & reimbursement, and patient advocacy colleagues. She/he will also represent Regeneron towards collaborators such as health care practitioners, research groups, payers and alliance partners.A typical day might include the following:
  • Develops and supervises implementation of US and ex-US focused medical strategy and tactics for one asset, including scientific communications and publications, annual medical planning, field communications, and collaborations with specialists.
  • Applies disease area expertise and business understanding to address needs in clinical practice with medically appropriate use of medicines.
  • Lead all aspects of and provides hands on support in management, generation and dissemination of clinical and non-clinical data that results in high quality publications.
  • Leads a cross-functional team and continuously strives for alignment across the organization (and the alliance if applicable).
  • Provides scientific/medical perspectives to the global and US strategic and medical organizations.
  • Co-leads the formation and execution of a robust Phase IIIb/IV plan
  • Supports the design, conduct, oversight, analysis and reporting of clinical trials. Ensures timely submission and delivery of high-quality clinical trial documentation, implementation and execution.
  • Continues to develop and nurture long-term strategic partnerships with clinical specialists, societies, collaborative groups, advocacy groups, and other external partners representing Regeneron.
  • Prioritizes support of investigator-initiated studies and serves as the Chair on an internal Scientific Review Committee.
  • Reviews and approves all promotional materials.
  • Ensures goals and objectives are met and projects completed on time and within budget.
  • Optimizes medical affairs resource prioritization across the spectrum of a product's life cycle.
  • Develops and forecasts of project budgets across assets.
  • Champions compliance, ethics and patient safety, putting patients at the center of all actions.
  • Monitors post-registrational trials and is the signatory of documents related to interpretation of patient level data where vital, if trained in medicine
This role might be for you if:
  • You work optimally in a fast paced, constantly evolving and growing environment.
  • You have outstanding work ethic and integrity, including high ethical and scientific standards
  • You handle scientific concepts and complexity with confidence.
  • You make the best decision possible based on a mixture of data analysis, wisdom, experience and judgment.
  • You establish and maintain effective working relationships with co-workers and gain their trust and respect.
  • You build a climate in which people want to do their best and can empower team or project members.
  • You deal comfortably with senior management.
  • You act upon the things you see as complicated.
To be considered for this opportunity an advanced degree (MD, PhD or PharmD) is strongly preferred. A minimum of 10 years of related industry experience in ophthalmology is required.

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.