Associate Director, Global Clinical Physician - Neuroscience

Working with Us Challenging. Meaningful. Life‑changing. At Bristol Myers Squibb, you will work on projects that transform patients’ lives and career trajectories. You’ll experience growth through opportunities uncommon in scale and scope, alongside high‑achieving teams. We value balance and flexibility. We offer competitive benefits to support both work and personal life. For more information, visit careers.bms.com/working-with-us. Functional Area Description The Associate Director, Global Clinical Physician is part of Clinical Development, a global organization dedicated to design, execution, and interpretation of clinical trials. Position Summary / Objective Primary medical accountability and oversight for clinical trials. Matrix management across internal and external networks. Strategic decision‑making for Phase 1‑Phase 3 studies. Provide medical and scientific expertise to cross‑functional BMS colleagues. Position Responsibilities Medical Monitoring Key member of a high‑performing Study Delivery Team (SDT) and Clinical Development Team (CDT). Review of trial data and eligibility. Coordinate site interactions with Global Clinical Scientist for medical questions and education. Assess serious adverse events and oversee safety narratives with Worldwide Patient Safety. Contribute to protocol development with medical strategic oversight. Maintain GCP compliance and required training. Clinical Development Expertise & Strategy Design and develop clinical plans and protocols that align with regulatory disease strategy targets. Provide oversight and accountability for a group of studies. Analyze benefit/risk in a matrix team environment. Support study execution with CS: site activation, enrollment status, adjudication of protocol deviations. Identify and collaborate with principal investigators and thought leaders to shape study design. Maintain in‑depth disease‑area expertise and stay current with scientific developments. Monitor competitive landscape and support pipeline positioning. Provide ongoing medical education in partnership with CS. Health Authority Interactions & Publications Support key Health Authority interactions and advisory board meetings. Author clinical content for CSRs, regulatory reports, briefing books, and submission documents. Degree Requirements MD required (or U.S. equivalent). Experience Requirements At least 3 years of industry or clinical trials experience. Key Competency Requirements Clear communication and presentation in scientific and clinical settings. Subspecialty training in applicable therapeutic area desired. Expertise in scientific method, statistical design, analysis, and interpretation. Knowledge of drug development process and effective clinical plan components. Strong leadership skills and teamwork. Travel Required Domestic and international travel may be required. Compensation Overview Salary ranges (est.): Cambridge Crossing $273,210–$331,063; Madison, Giralda, NJ $243,930–$295,589; Princeton, NJ $243,930–$295,589. Additional incentive cash, stock, and other benefits may be available. Benefits Health Coverage: Medical, pharmacy, dental, and vision care. Well‑being Support: BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs. Financial Well‑being and Protection: 401(k), disability, life insurance, supplemental health, travel protection, liability protection, identity theft, legal support, survivor support. Work‑Life Benefits Paid Time Off, including flexible time, paid national holidays, and optional holidays. Unlimited paid sick time, volunteer days, summer hours flexibility, leaves for medical, personal, parental, caregiver, and bereavement needs. Candidate Rights BMS will consider applicants with arrest and conviction records in compliance with applicable laws. Data Protection We never request payments or personal financial information during the application process. Learn more at careers.bms.com/fraud‑protection. #J-18808-Ljbffr