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The Associate Director, Clinical Supply Project Manager (Program CSPM) works in Global Clinical Supply (GCS) Planning, which manages the end-to-end integrated clinical supply chain across the Research & Development portfolio. Planning serves as a key interface between clinical development teams and the operational organizations responsible for clinical supply execution. The Program CSPM is the program-level GCS Planning point of contact for internal and external customers and the lead GCS spokesperson at clinical and development-related meetings. Working independently, the position designs strategic and operational plans for clinical supply activities across assigned compounds or programs. It coordinates with clinical development, regulatory, quality, and supply chain partners; establishes bulk manufacturing and drug-product release timelines; manages forecasts and bulk supply allocation; and identifies and escalates significant supply risks. The role is accountable for program clinical supply budgets and supports protocol and program cost estimates, documentation for labeling, packaging, and critical CMC activities, and collection of supply-chain metrics. The position also contributes subject-matter expertise to non-pipeline activities, mentors team members, supports staff development, and drives continuous improvement in clinical supply planning processes and systems. It contributes to departmental strategy and cross-functional projects, while applying sound judgment to unstructured problems and balancing strategic planning with tactical execution. The role emphasizes customer and patient focus, disciplined decision-making, ethics, and integrity.
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Job Type
Full-time
Career Level
Senior

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