Associate Director, Clinical Supply Chain

Role: Associate Director, Clinical Supply Chain, overseeing investigational medicinal product supplies for Eikon Therapeutics' global clinical-stage trials. Responsibilities include translating clinical study requirements into demand plans, managing supply logistics at CMOs and depots, leading supply chain execution, and serving as a primary liaison to clinical operations and CMC teams. The role also involves risk management, budget oversight, regulatory compliance, and documentation for GxP environments. Qualifications: 10+ years of experience in clinical supply chain management with a Bachelor's degree, or 8+ years with a post-graduate degree; expertise in clinical supply chain operations, manufacturing, quality, or regulatory functions preferred. High-value: extensive GxP knowledge, global clinical trial experience, supply chain planning, and vendor management; familiarity with IND/IMPD/CTA filings, validation, and drug development processes. Work setup and travel details are not specified, but the position demands cross-functional collaboration and adaptability in a fast-paced, matrixed environment.