Associate Director, Global Medical Cardiovascular, Mavacamten

Position Summary

The Associate Director, Global Medical Mavacamten is a key medical contributor responsible for driving the execution of the Global Medical plan for mavacamten across its lifecycle in hypertrophic cardiomyopathy (HCM). The role focuses on enabling US medical execution, providing scientific and clinical leadership across global deliverables—including core content and scientific materials, congress planning support, medical education, and cross‑functional scientific engagement—to ensure timely, high‑quality support for US priorities and milestones.

• Drive execution of the Global Medical plan for mavacamten, translating priorities into clear deliverables, timelines, and cross‑functional ways of working.
• Partner with Medical Market Leads to enable execution of US medical plans by providing global toolkits, scientific resources, and implementation support.
• Coordinate day‑to‑day cross‑functional alignment (Medical Communications, Clinical Development, Regulatory, Safety, Market Access) to manage dependencies and ensure on‑time, compliant execution of medical deliverables.
• Serve as a medical subject matter expert in hypertrophic cardiomyopathy, monitoring the external landscape and incorporating new insights into global materials that support US needs.
• Own assigned execution work streams ensuring materials are medically accurate, consistent, and usable for global and US deployment.
• Provide scientific guidance and clinical context to support execution decisions across internal stakeholders, escalating risks/issues as appropriate.
• Execute elements of the global and US publication/content plan, supporting medical review of abstracts, manuscripts, congress materials, and external scientific resources (promotional and non‑promotional, as required).
• Support global and US congress planning and execution by coordinating scientific content development, internal reviews, and readiness activities to meet timelines.
• Support execution of the Thought Leader Engagement Strategy by coordinating planning, materials, and follow‑up for key interactions (e.g., Advisory Boards) in partnership with US and regional teams, ensuring appropriate governance and transparency.
• Coordinate with cross‑functional partners to ensure scientific engagement strategies are aligned, compliant, and appropriately governed.
• Act as a core member of the Global–US mavacamten medical and commercialization matrix teams, representing global execution work streams and ensuring connectivity to US needs.
• Demonstrate strong cross‑functional leadership in a matrixed environment, influencing without authority and driving timely alignment across Medical, Clinical Development, Regulatory, Safety, Market Access, Marketing, and Commercial teams.
• Support medical training by developing and maintaining global training assets and ensuring consistency of scientific messaging used by US teams.
• Ensure all worldwide and US medical activities comply with company policies, applicable laws/regulations, and medical governance standards.

• Advanced scientific degree (MD, PhD, PharmD, PA/NP).
• At least 5+ years of experience in Medical Affairs within pharmaceutical or biotech with increasing responsibility.
• Experience in a global medical role supporting US execution strongly preferred.
• Cardiovascular disease expertise required; HCM or rare disease experience strongly preferred.
• Demonstrated success partnering cross‑functionally in complex, matrixed organizations.
• Prior industry experience in cardiovascular (CV) medical affairs/medical strategy, product launch, clinical research, or related experience is preferred.
• Must have experience working in a multi‑functional project team and managing external agencies.
• Proven ability to plan and implement medical congresses and advisory boards.
• Familiarity with all phases of drug development is desirable.

• Strong scientific and clinical acumen with the ability to translate data into actionable medical strategy.
• Ability to work effectively with cross‑functional teams including clinical, commercialization, regulatory, and early discovery.
• Highly professional with excellent…