Associate Director, Clinical Supply Chain

Role: Associate Director of Clinical Supply Chain responsible for overseeing the end-to-end management of clinical trial materials for IDEAYA's oncology programs. Objectives include ensuring robust, compliant supply chain operations supporting phase 1-3 global oncology trials, including supply planning, vendor management, packaging, labeling, distribution, return, and destruction of investigational drugs. Core responsibilities encompass managing external partners (CMOs, depots, couriers), developing supply policies, overseeing IRT systems, coordinating global shipments, and supporting regulatory compliance. Qualifications: BA/BS in Supply Chain, Engineering, or life sciences; 10+ years in biotech/pharma with 7+ years in clinical supply chain, including experience with CMC operations, IRT systems, and global oncology trials. Skills include supply forecasting, inventory management, GMP/GDP/GCP knowledge, cross-functional collaboration, and vendor management. Preferred: Certifications like APICS, PMP, experience with drug labeling, and international shipment. High-Value: Oncology, phase 1-3 trials, global distribution, biologics or small molecules, regulatory compliance, IRT, and GMP/GDP standards. Work setup: Onsite in South San Francisco, with 5-10% domestic travel.