Associate Director, Clinical Supply Chain

Role: Associate Director, Clinical Supply Chain at Olema Oncology, responsible for planning, developing, and optimizing the global clinical supply chain to ensure continuous drug supply for ongoing Phase 3 breast cancer trials. Key responsibilities include managing inventories, shipping, third-party vendors, developing IRT systems, overseeing packaging, labeling, distribution, identifying and mitigating supply risks, and collaborating with Clinical Operations to align supply demands. Qualifications: Bachelor's degree required (Master’s preferred), with 8+ years in biotech/pharma clinical supply chain management, especially in late-stage oncology trials involving small molecules; extensive experience in inventory management, global logistics, GMP standards, and clinical labels. Preferred skills include hands-on knowledge of IRT, QMS, and purchasing systems, along with strong project management, communication, and problem-solving abilities. High-value biopharma specifics encompass late-phase (Phase 3) clinical development, small molecule oncology drugs, GMP compliance, and global logistics expertise. The role reports to the VP, Clinical Supply Chain, and involves approximately 15% travel, with remote or hybrid work options available in San Francisco or Cambridge.