Medical Director, Medical Affairs-Dermatology Expert

4 weeks ago

Tarrytown, New York, United States Regeneron Pharmaceuticals Full time
Job Summary

We are seeking a highly skilled Medical Director to lead our Dermatology medical strategy and medical affairs activities. As a key member of our Medical Product Team, you will be responsible for developing and executing medical strategies, collaborating with internal and external stakeholders, and ensuring the delivery of high-quality medical communications and publications.

Key Responsibilities
  • Develop and lead all aspects of medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations within the healthcare community.
  • Apply therapeutic/disease area expertise and business understanding to address current and future medical needs in clinical practice with medically appropriate use of investigational medicines.
  • Oversee and provide hands-on support in management, generation, and dissemination of clinical and non-clinical data and results in high-quality publications.
  • Provide scientific/medical perspectives to the global and US strategic and medical organizations.
  • Support the design, conduct, oversight, analysis, and reporting of Medical Affairs clinical trials.
  • Continuing to develop and cultivate long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external collaborators representing.
  • Prioritize support of investigator-initiated studies and serve as a key member of internal Scientific Review Committees.
  • Ensure accuracy of training material for scientific and product information.
  • Coordinate medical review and approval of promotional materials.
  • Ensure goals and objectives are met and projects completed on time and within budget.
  • Responsible for optimal medical affairs resource allocation across the spectrum of a product's life cycle.
  • Oversee development and forecasting of project budgets across assets.
  • Perform medical monitoring of post-registrational trials and be the signatory of documents related to interpretation of patient-level data where necessary.
Requirements
  • Medical degree (MD/MBBS or equivalent) with 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.
  • Demonstrated experience leading technical and business discussions internally and externally and explaining 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.
About Regeneron Pharmaceuticals

Regeneron Pharmaceuticals 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.

The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

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