Global Medical Director leading medical strategy execution for Rare Hematology products at Sanofi. Driving evidence generation and expert outreach for critical healthcare advancements.
Responsibilities
Develop and execute the global medical affairs strategy for the Rare Hematology products
Ensure a patient-centric approach to development of medical affairs activities
Lead medical affairs data generation activities, including the development of study protocols, management of company sponsored clinical studies and real-world evidence studies
Provide medical expertise for medical education activities and publication plans
Establish and maintain strong relationships with experts in the relevant disease area
Organize and lead medical insight gathering activities (e.g., advisory boards) per the medical affairs plan
Review externally facing promotional and medical materials
Provide expertise and guidance to country medical teams to ensure outstanding scientific engagement globally and to help enhance medical education
Responsible for budget planning of medical activities
Provide medical expertise and input into Global Marketing, Market Access, and HEVA projects
Contribute as a medical expert to regulatory interactions and document development
Travels (both internationally and within the US) as necessary
Requirements
Medical doctor required (i.e., MD or MD/PhD), with post-graduate training (e.g., residency, fellowship)
At least 10 years of experience combining pharmaceutical industry and/or healthcare clinical practice
A solid track record of peer reviewed scientific publications, including expertise in Rare Diseases as a clinical researcher and/or as a clinician caring for patients with inborn errs of metabolisms
Previous clinical care experience on rare diseases or hematology
Excellent communication and presentation skills, with the ability to present scientific data in a clear, credible, and balanced manner
Able to interface professionally with a wide spectrum of internal and external clinicians, clinical researchers, regulatory agencies, HTA, payers, and industry executives in the scientific/medical arena
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