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 seamless and timely drug supply for oncology clinical programs, primarily in late-phase trials. Responsibilities include managing inventories, shipping, third-party manufacturing and logistics, developing IRT systems, overseeing packaging, labeling, and distribution, and identifying supply chain risks. The role partners closely with Clinical Operations and represents supply chain on study teams. Qualifications: Bachelor's degree required, Master’s preferred; 8+ years in biotech/pharma clinical supply chain, with experience in inventory management, global shipping, GMP compliance, and late-stage studies, particularly in oncology with small molecules. Skills include project management, problem-solving, and strong communication. Attributes: analytical, adaptable, collaborative, ethical, self-motivated, and results-driven. Location: San Francisco or Cambridge, with approximately 15% travel. High-value specifics: focus on late-phase oncology trials, global logistics, IRT development, GMP standards, and managing supply for multiple studies. Compensation: $185,000-$200,000 base salary, plus equity, bonus, and benefits.