Director, Clinical Supply Team Lead (CSTL)

Bristol Myers Squibb•Princeton, NJ

22h•$198,070 - $240,011•Hybrid

About The Position

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: careers.bms.com/working-with-us. The Director, Clinical Supply Team Lead is responsible for operational leadership and coordination of clinical supply activities across an assigned Therapeutic Area (TA). This role ensures consistent, high‑quality execution of planning, supply readiness, and asset/study support by directing Supply Asset Leads (SALs), Trial Supply Managers (TSMs), and other subordinate staff. The Director manages incoming assets and workload through a structured intake process, supports cross‑functional alignment, drives operational discipline, and ensures transparency through TA‑level metrics and dashboards. This role partners with senior leaders in GDO, CMC, Regulatory, Quality, GLS, CSO, and other CSC stakeholders to promote collaboration and strategic foresight as well as to ensure timely decision‑making, appropriate issue escalation, and operational risk mitigation across the TA portfolio. The Director promotes consistent ways of working, contributes to continuous improvement efforts to strengthen end‑to-end clinical supply performance, and supports the development of future-ready talent within their assigned TA.

Requirements

Bachelor’s degree in Supply Chain, Pharmacy, Life Sciences, Engineering, or a related field.
12+ years of experience in clinical supply chain, clinical operations, technical operations, or related fields.
Demonstrated experience in planning, study support, forecasting, or operational leadership in a GxP environment.
Demonstrated ability to effectively collaborate with and influence cross-functional people/teams to accomplish clinical supply goals and objectives
Strong understanding of investigational product supply, clinical study operations, and functional interfaces (CMC, Regulatory, Quality, GDO).
Proven ability to allocate resources, balance workload, and lead cross‑functional issue resolution.
Strong analytical skills and experience interpreting planning data, operational metrics, or dashboard insights.
Ability to lead through influence, support change adoption, and maintain consistent operational discipline.
Ability to coach, engage, and develop team members.
Experience managing change in a dynamic, complex environment.

Nice To Haves

Experience managing clinical supply chain professionals.
Experience with supply planning or S&OP processes (CD&OP experience desirable).
Familiarity with digital supply chain tools (i.e. IBP, Lighthouse, Control Tower, CASSA).
Prior experience supporting portfolio‑level planning or multi‑study coordination.
Excellent cross-functional negotiating skills.

Responsibilities

Lead TA level intake for new studies, new assets, and major protocol changes including IRT awareness of changes, comparator needs, CMC driven supply requirements, and similar clinical supply activities.
Assign and monitor assets across SALs, TSMs, and other team members based on capacity, expertise, study tiering, and other relevant data.
Maintain a forward‑looking TA portfolio view to anticipate workload shifts and evolving resourcing needs.
Ensure decisions and assignments are clearly documented and communicated within the TA as well as across CSC and partnering functions.
Ensure consistent execution of end‑to-end clinical supply planning and forecasting in close collaboration with SALs and TSMs.
Drive adherence to standardized processes/playbooks, escalation pathways, and governance expectations, recommending improvements as warranted.
Act as the first point of resolution for cross‑study conflicts, operational trade‑offs, and timeline risks.
Partner with GLS and CSC planning functions to ensure supply reliability, logistics coordination, issue resolution, and similar outcomes.
Acts as the main Clinical Supplies contact person for the assigned compound and associated studies, leading communications regarding global supply strategy with study team as appropriate.
Ensure early visibility of upcoming/emergent changes (e.g., protocol amendments, enrollment escalations, site activations, country expansions) and coordinate timely CSC response.
Facilitate regular TA operational review meetings to align stakeholders, assess resource allocations, track risks, and drive timely decisions.
Leverage KPI dashboards to enable proactive issue identification and drive top-tier performance..
Use Control Tower / E2E supply data to trend performance, identify bottlenecks, anticipate resource swings, and apply corrective actions.
Contribute to improving CD&OP maturity by reinforcing consistent inputs, process discipline, and cross‑functional engagement. More tactically ensure the appropriate projects are being escalated up the CD&OP process to achieve rapid resolution.
Ensure all TA operations comply with GxP, inspection readiness expectations, and CSC quality processes.
Provide day‑to-day coaching, guidance, and development for direct reports as well as SALs, TSMs, IPCs, and CFLs as needed across CSC.

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.
Work-life benefits include: 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. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.

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