Jobs · Business Development · New Jersey

Associate Director, Global Medical Cardiovascular, Mavacamten

Bristol Myers Squibb · Princeton, NJ · 4 wk ago
HybridBusiness Development$166k–$202k/yrFull-time

Position Summary

The Associate Director, Global Medical Mavacamten is a key medical contributor responsible for driving execution of the Global Medical plan for mavacamten across its lifecycle in hypertrophic cardiomyopathy (HCM), with a primary focus on enabling US medical execution.

Key Responsibilities

  • 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 (e.g., Medical Communications, Clinical Development, Regulatory, Safety, Market Access) to manage dependencies and ensure on-time, compliant execution of medical deliverables
  • Own assigned execution workstreams 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
  • Cover coordination 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 workstreams 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

Qualifications & Experience

  • 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
  • Experience working in a multi-functional project team and managing external agencies
  • Prior experience working in congress planning and execution
  • Familiarity with all phases of drug development is desirable

Skills & Competencies

  • 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 relationship-building and communication skills, including the ability to articulate complex scientific concepts verbally and in writing
  • Attention to detail with excellent planning, time management and organizational skills
  • Resilience and strong adaptability to change
  • Innovative and entrepreneurial thinking
  • Functions with excellent judgment, high integrity and in compliance with all laws, regulations, and policies

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