Associate Director, Clinical Supply Chain

Location: Redwood City, CA, United States Date Updated: Oct 27, 2026 Job ID: 18612 Description Senior Manager/Associate Director, Clinical Supply Chain The Role: You will play a critical role within the Pharmaceutical Development and Manufacturing organization, planning and delivering clinical supplies to support the company's clinical development programs. This is an on-site role based in the Bay Area. You must reside in the Bay Area or be open to relocating to the Bay Area. Key Responsibilities: Will be the clinical supply lead for assigned program(s) and develop/manage the clinical supply plan. Plan and deliver on-time, compliant clinical supply per the clinical development plan. Lead and manage clinical supply and logistics activities, for blinded as well as open label studies, including but not limited to; demand forecasting and supply planning, IRT start-up and maintenance, label generation and approval, packaging and labeling operations, release and distribution, expiry extension, cold chain management, and inventory management. Experience/Education: BS or MS in scientific fields with 8+ years of experience in clinical supply chain and logistics. Working knowledge of import and export laws and processes. Experience managing clinical supply activities for global phase 3, randomized, oncology clinical trials. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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