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Director, Admilparant Global Medical Strategy
Director, Admilparant Global Medical StrategyBristol Myers Squibb • Princeton, NJ, US
Director, Admilparant Global Medical Strategy

Director, Admilparant Global Medical Strategy

Bristol Myers Squibb • Princeton, NJ, US
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Director For Admilparant

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.

Position Summary

The Director for Admilparant will provide deep disease state knowledge in pulmonary disease (interstitial lung disease, COPD) leadership and direction to the US / Global Medical team; work with the medical matrix to focus on strategy, planning, development, and implementation of the US / Global medical plan. The Director will report to the Senior Director, Admilparant Medical Program Lead.

Key Responsibilities

  • Support the execution of US / Global medical plan that is both product and disease specific in alignment with US Commercialization (USC) and WW Medical (WWM), translating USC and WWM strategies into effective US / Global Medical launch plans and life cycle management plans.
  • Identify US / Global Medical data generation strategies, collaborate with Medical Evidence Generation (MEG) to oversee the execution of the Investigator Sponsored Research (ISR) programs from concept through full execution, including reporting the evidence at scientific congresses, in peer reviewed publications, and proactive / reactive BMS communication tools.
  • Works with Senior Director on a variety of projects, provides independent thought and initiative in the further development of specific projects and ensuing presentations and status updates
  • Manages projects to completion, anticipating obstacles and difficulties that may arise, and resolving them in a collaborative manner
  • Attends major conferences and helps coordinate medical affairs activities at conferences
  • Responsible for the development and execution of projects that will provide more extensive background, and additional data / answers to questions in response to issues relative to commercial, scientific, or data needs
  • Serves as medical strategy point on select scientific issues / topics using expertise to develop scientific messages, inform strategy, create / update slide decks, and review scientific content and publication
  • Collaborates with the Senior Director and medical matrix in the development of Customer Impact Plan and ensures alignment of team activities
  • Regular communication with external thought leaders and internal field team to identify key insights and to provide medical education, support, and direction as appropriate
  • Partner closely with colleagues in Discovery, Translational, Clinical Research, Regulatory, and Health Outcomes to ensure the science of the pipeline products and marketed medicines are understood and communicated properly internally and externally.

Qualifications and Experience

  • MD / DO (Pulmonary Imaging / Clinical Pulmonology / Medical affairs experience preferred)
  • Must be familiar with all phases of drug development
  • Knowledge of Healthcare landscape knowledge & insight
  • Proven impact and influence with high impact national thought leaders
  • Excellent analytical skills demonstrated ability to identify and understand complex issues and problems and identify and query key findings from study data and publications
  • Organized, attention to detail and ability to meet timelines in a fast-paced environment
  • Experience in developing effective abstracts, manuscripts, posters and slides, and presenting at scientific meetings
  • Ability to work on multiple projects simultaneously and effectively prioritize workload
  • Must be able to work with a level of autonomy and independence have business acumen and ability to partner and collaborate
  • Influencing and persuasion- negotiation skills
  • Strong verbal & written communication skills
  • Ability to lead and manage a complex (e.g., cross-functional, matrix designed) project team and change leadership
  • Experience with people management
  • Expected 30% travel within the continental US
  • Role is based in Princeton, NJ
  • 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 decided based on demonstrated experience. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following : Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility / infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program.

    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.

    On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role : Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

    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. Visit careers.bms.com / eeo-accessibility to access our complete Equal Employment Opportunity statement.

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