Lead development and execution of integrated Worldwide and US medical strategies for mavacamten across indications and lifecycle stages
Partner closely with Medical Market Leads to translate global medical strategy into region - specific medical plans detailing clear executional priorities
Drive alignment across cross‑functional stakeholders to ensure medical strategy informs and is informed by development, regulatory, access, and commercialization considerations
Serve as a global and US medical subject matter expert in hypertrophic cardiomyopathy
Provide leadership for global and US content generation strategy, disease education strategy, and data interpretation
Act as a trusted cross‑functional medical advisor, providing clear scientific guidance and clinical context to internal stakeholders
Contribute to Worldwide and US evidence planning, including RWE, Phase 4 studies, registries, and investigator‑sponsored research as needed
Support global and US publication and content strategy, including review of abstracts, manuscripts, congress materials, and externally-facing resources. Participate in medical review processes for promotional and non‑promotional materials, as required
Provide medical leadership for global and US congress strategy and execution
Partner with Global, US and regional medical teams to establish and maintain long-term Thought Leader Engagement Strategy. Manages Global Thought Leader activities, including Advisory Boards - aligns with functions, markets, and regions to ensure transparency regarding TL activities
Coordinate with cross‑functional partners to ensure scientific engagement strategies are aligned and appropriately governed
Act as a core member of the Worldwide-US mavacamten medical and commercialization matrix teams
Demonstrate strong cross‑functional leadership in a highly matrixed environment, influencing without authority and driving alignment across Medical, Clinical Development, Regulatory, Safety, Market Access, Marketing and Commercial teams
Support medical training initiatives and ensure consistency of scientific messaging across Global and US teams
Ensure all Worldwide and US medical activities comply with company policies and medical governance standards
Demonstrated success partnering cross‑functionally in complex, matrixed organizations
Prior industry experience in CV Medical affairs/Medical Strategy, Product launch and Clinical Research or related experience is preferred.
Must have experience working in 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
Skills & Compe
Additional Information
Working with Us
Challenging. 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 Summary
The Director, Global Medical Cardiovascular, Mavacamten is a key medical leader responsible for shaping and executing both Worldwide and US medical strategy for mavacamten across its lifecycle in hypertrophic cardiomyopathy (HCM). This role provides scientific and clinical leadership across global and US medical initiatives, including medical strategy development, evidence planning, publications, congress strategy, medical education, external communications, and cross‑functional scientific engagement.
The Director leads in a highly collaborative environment with a diverse matrix team. The Director partners closely with Regional Market Medical, Medical Communications, Clinical Development, Regulatory, Safety, Market Access, Marketing and Commercial teams, requiring strong cross‑functional leadership to ensure medical strategies are aligned, scientifically rigorous, clinically meaningful, and responsive to the evolving HCM landscape.
Bristol-myers Squibb · Princeton, NJ