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 uninterrupted drug supply for late-stage oncology trials. Responsibilities include managing inventories, shipping, third-party manufacturing, and logistics; developing IRT systems; overseeing packaging, labeling, distribution, and risk mitigation; and partnering with Clinical Operations to align supply with study demands. Qualifications: Bachelor's degree required, Master’s preferred; 8+ years in biotech/pharma clinical supply chain management, with expertise in GMP, inventory control, global shipping, and late-phase trials, particularly in oncology with small molecules. Attributes: strong communication, analytical and problem-solving skills, project management proficiency, entrepreneurial mindset, and high ethical standards. High-Value: Oncology, late-stage clinical development, global logistics, IRT development, GMP compliance, and experience with large, late-stage studies. Location: San Francisco or Cambridge, with approximately 15% travel.