Associate Director Clinical Supply Management

Job Summary

A company is looking for an Associate Director, Clinical Supply Management to oversee the clinical trial material supply for oncology studies.

Key Responsibilities

• Manage end-to-end supply chain strategies for clinical supplies across oncology studies
• Develop and maintain supply plans, manufacturing, and packaging schedules
• Provide oversight for packaging and distribution partners and ensure compliance with regulations

Required Qualifications and Education

• BA/BS with 3-5 years of experience in Clinical Supply Management or related field
• Solid understanding of pharmaceutical development, manufacturing, and global distribution
• Working knowledge of cGMPs, GCP, and applicable international regulations
• Experience with third-party vendors and contractors in clinical trials
• Global experience with phase 1-4 clinical trials