Director WW Medical, Pulmonology/Admilparant

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 Summary:The Director in WW Medical works in the WW Medical organization as a central part of the medical matrix team specifically functioning as the Co‑Lead for the Admilparant U.S. Launch.  The Director will play a central role in shaping, executing, and elevating the U.S. medical strategy for Admilparant as it prepares for successful Phase 3 readout and launch in idiopathic pulmonary fibrosis (IPF) and progressive pulmonary fibrosis (PPF). This leader will oversee medical launch readiness, evidence generation, scientific communications, and thoughtleader engagement in close partnership with the Worldwide (WW) Medical Team, U.S. Commercial, Market Access, Clinical Development, and crossfunctional partners. This role requires strategic thinking, scientific depth, matrix leadership, and the ability to operationalize a cohesive national launch plan that positions Admilparant as a transformative therapy in pulmonary fibrosis.  This individual will set clear and challenging targets that allow skilled and empowered professionals to accomplish business objectives consistent with department/program goals. This position requires objective and effective decision making, communication and presentation skills, desire and adeptness to work within a matrix team, and the ability to successfully manage and execute integration points across the global functional and commercialization areas to ensure alignment.  Key Responsibilities:Serve as Medical Lead for the U.S. Admilparant launch, accountable for end-to-end medical execution.  Lead the U.S. medical launch plan, ensuring alignment with WW Medical and Global Commercial; track progress, identify gaps, and implement mitigation.  Drive medical readiness across evidence generation, field capabilities, omnichannel education, and external engagement.  Anticipate and address emerging scientific, competitive, and clinical dynamics to strengthen market preparation.  Lead development and matrix execution of an integrated medical plan—both productspecific and diseasefocused—aligned with Global Commercial and WW Medical strategies.  Oversee medical data generation, including Phase 4 and ISR planning, publication delivery, and establishing BMS leadership in the therapeutic area.  Build and maintain strong relationships with global key opinion leaders, professional societies, and external partners through scientific exchange.  Lead strategic planning and content development for scientific advisory boards.  Oversee strategic planning of medical activities at major professional meetings and congresses.  Evaluate scientific merit and strategic fit of new ISR concepts and manage the ongoing ISR portfolio.  Collaborate closely with Global Commercial and Access teams to integrate medical insights into commercialization and ensure cross functional alignment.   Key Qualifications & Experience: Advanced scientific degree preferred (MD, PhD, PharmD) or similar.Experience in Immunology or Pulmonology is preferred.Should be experienced in Medical Affairs (US and WW), preferred Medical Strategy, ideally with experience in medical launch leadership, for minimum 4 years. Prior pharmaceutical industry experience in clinical research is desirable.Therapeutic area scientific & clinical expertise.Familiarity with all phases of drug development, including clinical development, regulatory and life cycle management. Healthcare landscape knowledge & insight.Ability to impact and influence with high impact national TA leaders.Vision and strategic thinker.Business acumen.Partnering and collaboration.Strong interpersonal skills commensurate with the need to work closely with both external physicians/scientists and numerous in-house support groups.Ability to maintain the highest degree of confidentiality and integrity, represent the company’s high ethics, moral behavior, and professionalism.Demonstrated ability to maintain scientific credibility while executing the Medical Affairs plan, and to communicate scientific results and effectively respond to data queries from customers and/or consultants.Strong scientific analytical skills.Ability to work under pressure, and to maintain scientific excellence within timelines.Experience within previous industry positions.Excellent English language skills, spoken and written.Ability to collaborate and partner effectively as well as work independently.  Expected travel.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: $207,490 - $251,433 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