Medical Director, Medical Affairs (Oncology)

Regeneron Pharmaceuticals • Sleepy Hollow, WY

17d • Onsite

About The Position

The US Medical Director of Medical Affairs is responsible for the development of medical strategy, planning & execution of medical affairs activities. We provide scientific/medical leadership by understanding malignant Oncology (solid tumors). You will represent US Medical Affairs for our skin cancer program at cross-functional meetings, aligning and working collaboratively with the Headquarters Medical Affairs Medical Directors and other Medical Affairs functions. This position will require you to be on-site 4 days/week at our Sleepy Hollow, NY offices. We cannot offer a remote option. If eligible, we can offer relocation benefits. Your travel days do include days in the office. A typical day may include the following: • Defines US specific Oncology strategy, sets annual goals and ensures compliant execution of medical affairs activities. • Collaborate with field medical, providing support to clinical development and clinical research conducted such as the identification of medical centers of excellence and key investigators/sites. • Participate in US scientific engagement with external communities advancing scientific and medical understanding including the appropriate development and use of our medicines, the management of disease, and patient care. • Develops the medical strategy and content for local congresses, symposia, advisory boards and local engagements and facilitates and implements such activities. • Delivers scientific presentations to diverse audiences in local cooperative meetings, advisory boards and scientific engagement forums. • Provides appropriate medical input, while maintaining scientific integrity, to commercialization strategies in country and serves as the local medical representative at Global Commercialization teams. • Will act as a lead medical reviewer in the MRC for the local review and approval of promotional, educational and related materials ensuring medical/ scientific accuracy and fair and balanced representation. • Provides medical and scientific review to US IIS proposals, protocols and concepts during the monthly meetings. • Supports and reviews US specific pathways and clinical guidelines submission.

Requirements

• Can demonstrate effective medical communication skills.
• Have a thorough understanding of the US healthcare environment.
• Have been accountabilities for evidence generation, external engagement and internal advice within a Medical Affairs function
• Ability to lead business and technical discussions internally and externally and explain scientific/medical concepts to all levels.
• Healthcare professional with a PharmD, PhD, or equivalent (a physician/MD is preferred.)
• Expertise in Oncology (solid tumors) clinical, research and/or drug-development is required.
• Minimum of +7 years’ experience in the pharmaceutical industry and medical affairs is required.
• Ability and willingness to travel ~40% of the time with some international travel.

Responsibilities

• Defines US specific Oncology strategy, sets annual goals and ensures compliant execution of medical affairs activities.
• Collaborate with field medical, providing support to clinical development and clinical research conducted such as the identification of medical centers of excellence and key investigators/sites.
• Participate in US scientific engagement with external communities advancing scientific and medical understanding including the appropriate development and use of our medicines, the management of disease, and patient care.
• Develops the medical strategy and content for local congresses, symposia, advisory boards and local engagements and facilitates and implements such activities.
• Delivers scientific presentations to diverse audiences in local cooperative meetings, advisory boards and scientific engagement forums.
• Provides appropriate medical input, while maintaining scientific integrity, to commercialization strategies in country and serves as the local medical representative at Global Commercialization teams.
• Will act as a lead medical reviewer in the MRC for the local review and approval of promotional, educational and related materials ensuring medical/ scientific accuracy and fair and balanced representation.
• Provides medical and scientific review to US IIS proposals, protocols and concepts during the monthly meetings.
• Supports and reviews US specific pathways and clinical guidelines submission.

Benefits

• comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels!
• relocation benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Director
• Education Level: Ph.D. or professional degree