ASSIGNMENT:
The consultant would be responsible for providing subject matter expertise on all aspects of clinical trial warehousing, including inventory management, storage conditions, and distribution protocols. They would collaborate with cross-functional teams to develop strategies for efficient, compliant management of clinical trial supplies, ensuring adherence to regulatory requirements, quality standards, and Good Clinical Practice (GCP) guidelines. Additionally, they would oversee the receipt, handling, storage, and distribution of investigational medicinal products (IMPs), ensuring accuracy and timely delivery, while offering domain guidance on optimizing clinical trial protocols and supply chain logistics.