Associate Medical Director of US Evidence Generation

Participate in strategic planning by supporting the development and refinement of the US RWE strategic plan, ensuring alignment with broader Medical Affairs and cross-functional objectives Support data-driven refinement of the US RWE strategic plan, content and messages through analysis of key performance indicators (KPIs) related to knowledge, attitudes and practices of US stakeholders through advisory boards, field insight generation and feedback from professional medical associations Ensure coordination among matrixed teams including Medical Affairs, Commercial, Publications, Materials Review Boards, Compliance, and external partners to incorporate RWE findings into publications and field materials Participate in the development of abstracts, manuscripts, and presentations for scientific congresses and peer-reviewed journals Ensure all RWE activities comply with relevant Alnylam SOPs, US regulatory, legal, and ethical standards, including data privacy and local guidelines Advanced degree (PharmD, PhD, MD) with strong preference for candidates with experience in cardiology and/or RWE generation Minimum of 5 years of experience in medical affairs within the pharmaceutical or biotech industry, including experience in field medical roles, strategy development and evidence generation Excellent interpersonal, communication, and collaboration skills, with the ability to engage effectively with internal and external stakeholders Strong scientific acumen, ability to function autonomously, and succinctly communicate with cross-functional stakeholders Experience managing budgets and external partnerships related to RWE projects Experience supporting both product launches and lifecycle management with RWE Entrepreneurial spirit and resourcefulness Excellent project management skills Ability to travel as needed to fulfill job responsibilities