This role uses logistics experience to plan, document, and facilitate global cross-border supply strategies. This includes ensuring compliance with global trade standards and in-country permitting requirements for the delivery of products such as clinical specimens, supplies, and research materials to their final destinations. The coordinator will attend clinical project meetings to gather information and translate clinical trial protocol details into supply plans that meet critical timeline and budget targets. They will also provide risk-mitigation strategies to prevent delays or expenses in the supply chain, track shipment journey information using various tools to ensure material stability and timely delivery, build relationships with couriers, and ensure shipping materials are validated according to regulatory requirements.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed