Freelance Clinical Supply Coordinator

Job Summary

Supporting global clinical studies on a part-time basis, the Freelance Clinical Supply Coordinator will manage investigational medicinal product (IMP) oversight, supply forecasting, and documentation review while working remotely with a leading pharmaceutical sponsor.

Key Responsibilities

• Provide expert support for clinical trial supply activities on a part-time (0.1 FTE) basis
• Review and maintain IMP-related documentation to ensure quality, accuracy, and regulatory compliance
• Support supply forecasting activities to ensure adequate drug availability throughout study execution

Required Qualifications

• Bachelor's degree in Pharmacy, Life Sciences, Supply Chain Management, or a related field, or equivalent relevant experience
• Experience in Clinical Supply, Clinical Operations, Drug Supply Management, or Clinical Trial Management within the pharmaceutical, biotechnology, or CRO industry
• Understanding of clinical trial supply processes, IMP management, and GxP requirements
• Experience with supply forecasting, inventory planning, logistics coordination, or vendor management
• Ability to work independently and provide expert guidance in a fractional consulting capacity