Executive Director, Clinical Supply Portfolio Lead, HOCT
Bristol Myers SquibbAbout the role
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.
Position Summary:
This Executive Director, Therapeutic Area Lead will provide strategic direction and operational leadership for the clinical supply across Hematology, Oncology, & Cell Therapy (HOCT) portfolios, inclusive of all BMS products and 3rd party pharmaceuticals required to support all phases of development research and post launch label expansions across the globe. This role will report into the VP, Global Clinical Supply Chain and will lead the team responsible for developing and executing clinical supply strategies across all HOCT assets and studies, ensuring seamless execution to support global research and development. This position will lead supply forecasting, oversee planning & inventory management operations, and manage cross-functional teams, stakeholder relationships, and continuous improvement in supply chain processes with a focus on patient needs, priority studies, and regulatory compliance.
Key Responsibilities:
- Ensure consistent strategy development and implementation of integrated clinical supply strategies for the HOCT portfolio, ensuring alignment with organizational goals, regulatory requirements, and patient needs.
- Provide strategic direction and leadership to the HOCT Therapeutic Area organization.
- Oversee end-to-end clinical supply chain, including forecasting, planning, inventory management, packaging and labeling campaigns, distribution, site supply, and use date extensions.
- Ensure compliance with GxP, safety standards, and regulatory requirements across all clinical supply operations.
- Drive innovation and operational excellence by identifying and implementing process improvements, cost-saving initiatives, and strategic global programs or systems.
- Shape and optimize matrix team governance and execution, fostering a culture of continuous improvement and accountability.
- Instill a cost-conscious mindset across the organization, managing comparator/co-med budgets and minimizing waste.
- Lead resolution of senior-level escalations and issues with portfolio-wide implications.
- Communicate and align the therapeutic area strategy across cross-functional teams to ensure visibility and execution.
- Apply leadership development principles, ensuring staff development, succession planning, and a high-performance culture.
- Solve complex, cross-functional problems, evaluating fundamental issues and intangible variables to drive strategic decisions.
- Lead clinical supply planning activities for both BMS and non-BMS sponsored research, ensuring timely delivery of finished clinical supplies.
- Ensure the HOCT team are fully leveraging the capabilities of AI to drive meaningful improvement in ways of working, simplifying processes and releasing resources to focus on more critical areas
- Interface and collaborate across CSC TAs for aligned business practices and customer service.
- Establish key performance indicators that facilitate the identification of improvement opportunities and ensure successful realization of goals and objectives and delivery for the portfolio
- Partner with the GDO, finance and CSO organizations to operationalize the CD&OP process, to manage priorities, conflict resolutions across the BMS development processes.
Qualifications & Experience:
- Bachelor’s degree in Pharmacy, Life-Sciences, Supply Chain, Engineering, or related technical field; advanced degree (MBA, PharmD, etc.) preferred.
- 15+ years of experience in pharmaceutical industry, with significant expertise in drug development, clinical supply chain management, and/or clinical manufacturing
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