Associate Director leading medical information strategy for Regeneron’s therapeutic areas. Managing tactical execution of medical affairs plans and providing scientific support for healthcare professionals.
Responsibilities
lead scientific communication and medical information strategy for assigned therapeutic areas
manage the tactical execution of Global and US Medical Affairs medical information plans
develop and deliver high-quality, balanced, and scientifically accurate responses to medical inquiries
lead the creation and maintenance of deliverables, including literature reviews, Standard Response Documents (SRDs), verbal FAQs, Q&As, AMCP dossiers, and compendium
medical reviewer on Promotional and Medical Review Committees, ensuring medical accuracy, clarity, and compliance
own department reporting processes and dashboards
evaluate, pilot, and implement AI-enabled tools and technologies to streamline medical information processes
collaborate with global and regional Medical Affairs partners
provide scientific support for congress planning and booth activities
mentor and train new hires and less experienced colleagues
Requirements
minimum of 5 years of Medical Information experience within the pharmaceutical industry
PharmD or PhD required
strong scientific knowledge and expertise in a therapeutic area
demonstrated experience in conducting scientific literature review
management of medical inquiries including development and review of deliverables (e.g., standard response documents, FAQs, dossier, compendium submissions)
practical experience and knowledge of FDA guidance’s
experience in neurology preferred
Benefits
health and wellness programs (including medical, dental, vision, life, and disability insurance)
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