Associate Director, Global Medical Cardiovascular, Mavacamten in Uxbridge

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.
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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. 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 team that manages a diversified matrix 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 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.
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 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.
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 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.
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.

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.
Ability to navigate ambiguity and align a range of stakeholders around shared medical objectives.
Acts with the highest level of leadership with Enterprise Mindset and flexibility.
Attention to detail with excellent planning, time management and organizational skills.
Resiliency and strong adaptability to change.
High-level negotiation skills and the ability to resolve conflict in a constructive manner.
Innovative and entrepreneurial thinking.
Functions with excellent judgment, high integrity and in compliance with all laws, regulations, and policies.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:
Princeton - NJ - US: $166,350 - $201,571. The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment.

Our benefits include:
Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include: Paid Time Off.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com.

Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

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