Job Abstract

SUMMARY/POSITION OBJECTIVE:

The Medical Director, CV metabolic, General Medicine, Global Medical Affairs, will fulfill a meaningful strategic leadership role and has high visibility in the organization. They will lead the development of medical strategy, planning & execution of medical affairs activities at Regeneron with the benefit of the patient at the forefront. They will ensure medical activities are delivered with integrity and scientific accuracy. They will provide scientific and medical leadership and serve as a key scientific and medical resource.

The Medical Director will lead the Medical Impact Team (MIT) with global and US focused results. The MIT is a multifunctional team that is consisted of colleagues within the medical affairs group (including field medical, medical operations, medical education, medical information, HEOR, publication management and medical statistics). The Director will represent Regeneron global medical affairs and ensure alignment working closely with research & development, new product planning, access & reimbursement, and patient advocacy colleagues. They will also represent Regeneron towards external collaborators such as leading health care professionals, research groups, payers, and alliance partners. 

A typical day in this role might look like:  

• Develops and is responsible for implementation of medical strategy and tactics for Evkeeza and other CV/metabolic pipeline assets, including scientific communications and publications, annual medical planning, field communications, and collaborations with experts.
• Applies therapeutic/disease area expertise and clear business understanding to address current and future medical needs in clinical practice with medically appropriate use of investigational medicines.
• Coordinates and provides hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications.
• Works with a cross-functional team and continuously strives for alignment across the organization (and the alliance if applicable)
• Acts as standing or ad-hoc member for various cross-functional and cross-alliance teams; provides scientific/medical perspectives to the global and US strategic and medical organizations.
• Supports the design, conduct, oversight, analysis and reporting of Medical Affairs studies when applicable.
• Continues to develop and nurture long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external stakeholders representing Regeneron.
• Coordinates and conducts advisory board meetings.
• Prioritises for support of investigator-initiated studies and serves as a key member of internal Scientific Review Committees when appropriate.
• Ensures accuracy of medical material for scientific and product information 
• Leads all aspects of medical review and approval of promotional or non-promotional materials when applicable.
• Ensures goals and objectives are met and projects completed on time to high standards and within budget.
• Is responsible for development and forecasting of project budgets for responsible assets.
• Champions high standards of compliance, ethics and patient safety, putting patients at the center of all actions.

This role might be for you if:

• Medical degree essential (MD. / Ph.D. / PharmD.)
• 7 years of related industry experience in medical affairs
• Proven background and experience in drug development and life-cycle management
• Specialized knowledge: CV/metabolic and HoFH
• Ability to lead 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.
• Detailed understanding of the healthcare environment including all external stakeholders.