Bristol Myers Squibb · 2 months ago
Associate Director, Clinical Supply Program Leader
Madison - Giralda - NJ - US
Full-time
Hybrid
Lead/Staff, Director/Executive
$168K/yr - $203K/yr
10+ years expBristol Myers Squibb is a company dedicated to transforming patients' lives through science. The Associate Director, Clinical Supply Program Leader will strategize direction for clinical supply chain planning activities for assigned programs in the R&D Portfolio and act as a subject matter expert on the global use of investigational material in clinical studies.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Provides strategic direction for clinical supply chain planning activities for assigned programs in the R&D Portfolio
Serve as primary Clinical Supply Services point of contact on Development and Project Teams
Lead Clinical Supply Matrix Teams to develop integrated cross functional strategy and implementation plans to ensure a continuous supply of investigational product as outlined by Project Team strategies and objectives
Responsible for alignment of functional execution plans with approved supply strategies
Primary interface with governing bodies and responsible for communicating and implementing governance body decision
Ensure alignment between the project strategy and tactical execution of the supply plans
Assure coherence between the global supply strategy, Project Team objectives and Clinical Supply Chain management objectives
Provide overall project leadership to the Clinical Supply Matrix Teams:
Articulates a clear, compelling vision and direction for the team, linking it to the BMS mission
Clarifies team member roles and responsibilities, sets clear expectations holding team members accountable for meeting commitments and timelines
Creates a supportive environment of open communication and actively engages and listens to other viewpoints
Identifies and manages conflict resolution quickly and constructively
Establishes a clear framework for decision making so that team members are empowered and informed about the types of decisions made at the team level and at the governance/executive level
Manage and maintain study supply budgets, including IP and comparators, to align with study timelines and deliverables, with the support of functional partners, ensuring appropriate and timely resource allocation to achieve project goals
Leads end‑to‑end program forecasting, ensuring accurate projections of clinical supply needs based on enrollment trends, protocol changes, and portfolio priorities
Escalate issues in a timely fashion
Qualification
Required
Bachelor's degree in Pharmacy, Supply Chain Management, Business or Pharmaceutical Sciences
10+ years clinical supply chain or related operational planning/leadership experience
Experience in multiple functional areas (clinical, regulatory, quality, product development) demonstrating a broad understanding of pharmaceutical development
Expert knowledge of all phases of drug development, of the functions and processes relevant to drug development, and project management principles applicable to the biopharmaceutical environment
Extensive and planning and execution of investigational materials supply strategies
Demonstrated strategic and leadership skills
Proven ability to effectively develop, communicate, and gain support for execution plans with a wide range of stakeholders
Result oriented individual to execute strategy and meet objectives
Experience managing change in a dynamic, complex matrix environment
Strong background in cGxPs and ICH requirements
Excellent Cross-functional negotiating skills
Coaches team members
Influences key stakeholders outside of the team
Preferred
PMI PMP certification preferred
Benefits
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.
Paid Time Off
US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-25
The Motley Fool
2026-01-24
Company data provided by crunchbase