Associate Director, Global Medical Cardiovascular, Mavacamten

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.Position SummaryThe 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. This role provides 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.The Associate Director operates in a highly collaborative environment with a diverse matrix team and partners closely with US Medical, Regional Market Medical, Medical Communications, Clinical Development, Regulatory, Safety, Market Access, Marketing, and Commercial teams. The successful candidate will translate global plans into practical execution—coordinating inputs, managing timelines, and ensuring scientific accuracy and consistency of materials—so US-facing activities are aligned, clinically meaningful, and responsive to the evolving HCM landscape.Key ResponsibilitiesDrive execution of the Global Medical plan for mavacamten, translating priorities into clear deliverables, timelines, and cross-functional ways of workingPartner with Medical Market Leads to enable execution of US medical plans by providing global toolkits, scientific resources, and implementation supportCoordinate 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 deliverablesServe as a medical subject matter expert in hypertrophic cardiomyopathy, monitoring the external landscape and incorporating new insights into global materials that support US needsOwn assigned execution workstreams ensuring materials are medically accurate, consistent, and usable for Global and US deploymentProvide scientific guidance and clinical context to support execution decisions across internal stakeholders, escalating risks/issues as appropriateExecute 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 timelinesSupport 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 transparencyCoordinate with cross-functional partners to ensure scientific engagement strategies are aligned, compliant, and appropriately governedAct as a core member of the Global–US mavacamten medical and commercialization matrix teams, representing global execution workstreams and ensuring connectivity to US needsDemonstrate 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 teamsSupport medical training by developing and maintaining global training assets and ensuring consistency of scientific messaging used by US teamsEnsure all Worldwide and US medical activities comply with company policies, applicable laws/regulations, and medical governance standardsQualifications & ExperienceAdvanced scientific degree (MD, PhD, PharmD, PA/NP)At least 5+ years of experience in Medical Affairs within pharmaceutical or biotech with increasing responsibilityExperience in a global medical role supporting US execution strongly preferredCardiovascular disease expertise required; HCM or rare disease experience strongly preferredDemonstrated success partnering cross‑functionally in complex, matrixed organizationsPrior industry experience in cardiovascular (CV) medical affairs/medical strategy, product launch, clinical research, or related experience is preferredMust have experience working in a multi-functional project team and managing external agenciesProven ability to plan and implement medical congresses and advisory boardsFamiliarity with all phases of drug development is desirableSkills & CompetenciesStrong scientific and clinical acumen with the ability to translate data into actionable medical strategyAbility to work effectively with cross-functional teams including clinical, commercialization, regulatory, and early discoveryHighly professional with excellent relationship-building and communication skills, including the ability to articulate complex scientific concepts verbally and in writingAbility to navigate ambiguity and align diverse stakeholders around shared medical objectivesActs with the highest level of leadership with Enterprise Mindset and flexibility Attention to detail with excellent planning, time management and organ