Director, Global Medical Cardiovascular, Medical Product Lead NJ - US R1605170 Post

Position: Director, Global Medical Cardiovascular, Medical Product Lead NJ - US R1605170 Post[...]
## Director, Global Medical Cardiovascular, Medical Product Lead Princeton - NJ - USFind out how well you match with this job
** 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:
** Position Summary
** This position plays a critical role in the development and execution of BMS' WW & US medical strategy for a next-generation cardiac myosin inhibitor within the cardiovascular portfolio. The Medical Medical Product Lead (MPL) is a strategic leader with broad responsibilities across the Medical organization and a key leader of the cross-functional matrix, providing medical insights and interpretation of the evolving heart failure (HF) and cardiomyopathy landscape and translating emerging clinical and scientific data across the organization.

The MPL has overall accountability to develop aligned medical strategies and execute core medical deliverables, including Integrated Evidence Plans, Scientific Narratives, and External Engagement and Advocacy plans as the lead of the cross-functional Asset/Indication Medical Strategy (AIMS) team.

The Director, MPL will provide strategic oversight for a new asset in heart failure and cardiomyopathy, initially focused on heart failure with preserved ejection fraction (HFpEF) and future life cycle management opportunities. This leader will direct and navigate complex issues across a broad cross-functional matrix to ensure optimal medical affairs strategy is developed and executed, including clear differentiation, evidence strategies that address monitoring burden and safety margin, and internal positioning across the broader myosin inhibitor franchise.

This medical leader will report to the VP, Head of Cardiovascular Medical Affairs and work closely with CV global program leads in Clinical Development.
** Key Responsibilities
*** Develop and execute the WW & US Medical Affairs strategy, ensuring alignment with the overall BMS cardiovascular disease area strategy and the broader myosin inhibitor franchise.
* Act as the core global medical representative for WW & US program teams, providing strategic medical and scientific leadership across cross-functional forums.
* Lead the cross-functional Asset/Indication Medical Strategy (AIMS) team for, setting strategic direction and aligning medical deliverables across global markets.
* Shape and articulate a clear scientific differentiation narrative versus existing and emerging myosin inhibitors and modulators, including considerations related to pharmacokinetics, pharmacodynamics, titration, monitoring burden, safety margin, and physician confidence.
* Partner across Worldwide Medical, Development, Regulatory, Commercial, HEOR, and Access to ensure the asset is positioned appropriately within the BMS cardiovascular portfolio and that internal sequencing and franchise strategy are clearly defined.
* Develop and execute global medical strategy, scientific narratives, and insight plans that reflect the evolving treatment landscape, including competitive dynamics and emerging standards of care. This will be put in the context of the broader CV BMS cardiomyopathy franchise, with expected collaborations across the other asset teams.
* Lead work streams to identify evidence gaps and develop comprehensive Integrated Evidence Plans (IEPs), including strategies to assess clinically meaningful differentiation such as usability in practice, monitoring requirements, and safety profile.
* Establish and oversee global medical data generation strategies; collaborate with Medical Evidence Generation (MEG) to guide Investigator Sponsored Research (ISR) programs and other evidence-generation initiatives from concept through execution and dissemination.
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