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Job description
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
Managing external partners (CMOs, depots, couriers)
Developing supply policies
Overseeing IRT systems
Coordinating global shipments
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
Supply forecasting and inventory management skills
Knowledge of GMP/GDP/GCP
Cross‑functional collaboration and vendor management experience
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.
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Worksite address
south san francisco, CA, 94083, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.