$ cat jobs/associate-director-director-clinical-supply-chain-eu-codera-llc-32086ef38368.json
Associate Director/Director, Clinical Supply Chain (EU)
About Codera Codera is a Tang Capital company that provides in-house end-to-end drug development capabilities for its portfolio companies. Founded in 2002, Tang Capital is a life-sciences focused investment company that creates, acquires and finances companies that develop and commercialize pharmaceutical products. Position Summary The Associate Director/Director, Clinical Supply Chain will lead end-to-end clinical supply chain operations for assigned international studies. This role is responsible for supply planning, forecasting, packaging, labeling, and distribution management, as well as the oversight of key supply chain vendors — including shipping and logistics providers, clinical supply depots, and IRT vendors — from study start-up through close-out, while partnering closely with internal stakeholders to ensure clinical materials are available and that study strategies, timelines, and budgets are met. The ideal candidate brings extensive experience managing European and Rest of World (RoW) operations, including booklet label development, the Qualified Person (QP) release process, import/export logistics, and cold chain management. Essential Duties and Responsibilities Serve as the primary clinical supply chain contact for assigned studies Provide study- and site-level operational support, including resupply requests facilitation, returns and destruction oversight, and temperature excursion management Develop and execute global inventory supply plans in coordination with Technical Operations, Clinical Operations and Quality Assurance Lead label development efforts for assigned studies, including booklet label development for international studies Manage manual and IRT-enabled drug supply shipments Facilitate and oversee storage, returns, reconciliation and destruction Monitor inventory levels, drug product expirations and resupplies Oversee import/export licenses and customs forms Ensure batch release dates are properly prioritized for key study timelines Revi
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