Logistics Project Manager, Associate Director, Hybrid

Role: Manage global clinical supply logistics within the Clinical Supply organization, focusing on optimizing the end-to-end distribution process for clinical trials across the company’s research portfolio. Responsibilities: Collaborate with internal teams and external partners to improve supply chain efficiency, ensure compliance with GMP and GDP, oversee shipping documentation and customs processes, monitor logistics performance, and drive continuous process improvements. Qualifications: Bachelor’s Degree with at least 6 years’ experience in pharmaceutical supply chain or high school diploma with 10+ years’ relevant experience; strong knowledge of international shipping, supply chain systems like SAP, and clinical supply operations. High-Value: Focus on global clinical trial logistics, supporting investigational products for various phases, with compliance to GMP/GDP standards and regulatory requirements. Work Setup: Hybrid in the US with approximately 10% travel.