Clinical Supply Specialist II - Onsite in Aliso Viejo, CA

Role: Clinical Supply Specialist II supporting planning, coordination, and execution of clinical supply activities for assigned studies. Responsibilities: develop and execute supply plans including forecasting, inventory management, and distribution; coordinate investigational product shipments ensuring regulatory and quality compliance; collaborate with Clinical Operations, CMC, Manufacturing, Quality, and vendors to ensure supply readiness; monitor inventory levels, troubleshoot issues, and maintain documentation; contribute to process improvements and participate in supply chain meetings. Requirements: 2–5 years experience in clinical supply chain, clinical operations, or related fields; strong understanding of supply processes such as forecasting and logistics; experience supporting regulated clinical trials with investigational product handling; proficiency in supply systems (e.g., IRT); bachelor’s degree in biological sciences, health sciences, supply chain, or related discipline. High-Value: experience in clinical trial supply, regulated environments, logistics coordination, and supply systems; familiarity with GCP/FDA standards; onsite work in Aliso Viejo, CA. Work setup: onsite at headquarters.