Director, Medical Affairs

Advanced degree in a healthcare-related field (MD, PharmD, PhD, or equivalent). 7+ years of experience in medical affairs or related roles in the pharmaceutical or biotech industry. Experience supporting clinical trials and working cross-functionally in a matrixed environment. Strong scientific acumen, communication skills, and ability to work independently in a fast-paced setting. Strong understanding of regulatory and compliance frameworks (e.g., FDA, EMA).

Support development and communication of medical plans for the therapeutic area. Incorporate insights from scientific trends and treatment landscape by participating in external events and activities. Lead the development and dissemination of scientific and medical data through publications, presentations, and educational programs for healthcare professionals. Build and maintain strong relationships with KOLs, researchers, and patient advocacy groups. Manage conference calendar and coordination of onsite meetings. Coordinate logistics for advisory boards, symposia, and medical education events. Collaborate with internal regulatory team to ensure compliance with relevant regulations. Oversee or contribute to studies that generate real-world evidence (RWE), health economics and outcomes research (HEOR), and other data. Act as a scientific consultant and collaborator with internal teams including R&D, Clinical Development, Regulatory Affairs, and Commercial. Provide accurate and up-to-date medical information to address inquiries from HCPs and other external stakeholders. Manage medical review of promotional content and ensure compliance with MLR standards.