As Associate Director, Medical Information, you will lead scientific communication and medical information strategy for assigned therapeutic areas, enabling high-quality, compliant scientific exchange with healthcare professionals, patients, and internal team members. You will manage the tactical execution of Global and US Medical Affairs medical information plans, convert insights into strategic recommendations, and serve as a trusted partner while ensuring full adherence to company policies, procedures, and all regulations and industry standards. Location and Travel • On-site 4 days/week in Sleepy Hollow, NY or Warren, NJ• If based in Warren, NJ, occasional travel to Sleepy Hollow, NY is expected• Travel (up to 10% is expected) Responsibilities Develop and deliver high-quality, balanced, and scientifically accurate responses to medical inquiries; resolve complex and brought up inquiries. Lead the creation and maintenance of deliverables, including literature reviews, Standard Response Documents (SRDs), verbal FAQs, Q&A, AMCP dossiers, and compendium. Serve as medical reviewer on Promotional and Medical Review Committees, ensuring medical accuracy, clarity, and compliance. Own department reporting processes and dashboards, including metrics, insights generation, digital analytics, and trend reporting for internal partners. Evaluate, pilot, and implement AI-enabled tools and technologies to streamline medical information processes and improve efficiency and quality. Collaborate with global and regional Medical Affairs partners to ensure alignment and share best practices. Provide scientific support for congress planning, booth activities, and real-time scientific exchange. Mentor and train new hires and less experienced colleagues; may directly supervise Senior Managers, Specialists, and contractors. Qualifications 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, including evaluating and communicating clinical trial and disease state information to a wide range of audiences; Neurology is preferred. Demonstrated experience in conducting scientific literature review and managing medical inquiries, including the development and review of deliverables such as standard response documents, FAQs, dossiers, and compendium submissions. Practical experience and knowledge of FDA guidance. Benefits We offer a comprehensive benefits package that may 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. Salary Salary Range (annually): $157,200.00 - $256,600.00 Regeneron 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. #J-18808-Ljbffr