Manager, Clinical Supply Chain

Role: Clinical Supply Chain Manager for late-stage oncology trials supporting RAS(ON) inhibitors in global Phase I-III studies. Responsibilities: develop and execute clinical supply strategies, demand forecasting, inventory management, global packaging, labeling, distribution, and logistics; support IRT/RTSM systems; manage external vendors; implement risk mitigation and continuous improvement initiatives; oversee budgets and vendor performance; contribute to regulatory documentation. Requirements: Bachelor’s/Master’s in Supply Chain, Life Sciences, or related field; 5+ years managing global clinical supply chains in pharma/biotech; expertise in GCP, GMP, GDP, ICH, and regulatory standards; experience with clinical logistics, vendor management, and planning tools; strong leadership and cross-functional collaboration skills. Preferred: oncology development experience, late-stage supply management, cold-chain distribution, and process improvement leadership. High-Value: late-stage oncology, Phase I-III, global supply chain, regulatory compliance, IRT/RTSM systems, vendor oversight. WorkSetup: onsite at Redwood City, CA, with salary range $143K–$178K, plus benefits and equity.