Cell Therapy Clinical Product Administration Process Expert
7 days ago
Bristol Myers Squibb is a company that empowers its employees to apply their individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials. Our shared values of passion, innovation, urgency, accountability, inclusion, and integrity bring out the highest potential of each of our colleagues.
About the Role:
The Associate Director, Cell Therapy Clinical Product Administration Processes (C-PAP) is a key member of the Cell Therapy Franchise Organization who will work closely with the Cell Therapy Franchise, Global Drug Development, and all Cell Therapy cross-functional teams as an internal subject matter expert (SME) to build and ensure excellence as it relates to clinical trial product handling and administration. This Individual has a masterful understanding of the product handling and administration practices of Cell Therapy products across different phases of clinical trials.
Responsibilities:
- Provide subject matter expertise (SME) to key internal stakeholders on clinical trial product handling and administration across all phases of Cell Therapy clinical trials.
- Serve as a clinical trial product handling and administration SME to key internal stakeholders during the review and resolution of clinical events, quality reviews, and audit activity.
- Serve as a clinical trial product handling and administration SME to key internal stakeholders during the study startup phase and for the life span of a Cell Therapy clinical trial across early and late development.
- Collaborate with cross-functional partners on process improvement as it relates to Cell Therapy clinical trial execution and operations to achieve operational excellence and a successful execution of clinical trials at activated sites.
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