Responsibilities:
• Support development and execution of annual Medical Affairs strategic and tactical plans.
• Collaborate cross-functionally with Clinical, Commercial, Regulatory, and Field Medical to ensure alignment with scientific and business objectives.
• Operationalize and manage Medical Affairs activities such as advisory boards, symposia, scientific congress planning, and educational initiatives.
• Serve as a key Medical Affairs contributor on the Promotional Review Committee (PRC) and Medical Review Committee (MRC) to ensure scientific accuracy, compliance, and alignment with medical strategy.
• Support the planning and implementation of the Investigator-Sponsored Research (ISR) program, including proposal review, coordination of internal evaluations, and communication with investigators.
• Partner with Clinical Development to integrate healthcare provider insights and support the design and execution of clinical trials.
• Collaborate with Commercial colleagues on compliant alignment of strategy and assist with development of promotional materials including slide decks, FAQs, and internal training content.
• Help develop and maintain internal Medical Affairs processes, SOPs, and guidance documents.
• Gather, synthesize, and share scientific and clinical insights from KOL interactions, advisory boards, and scientific conferences.
• Assist in vendor oversight and budget management for assigned initiatives.