Clinical Trial Coordinator – Green Key Resources – Carlsbad, CA, USA

Qualifications 2+ years of experience in clinical logistics or similar pharmaceutical industry required

4+ years of experience in handling imports and exports necessary

Comprehensive understanding of clinical trial logistics necessary

Advanced working knowledge of IATA, DOT and Cold Chain UN-Packaging requirements and FDA and USDA import requirements, as well as DEA regulations necessary

Proven success in process improvement, problem solving, and policy writing required

Proficiency in Microsoft Office Suite necessary

Job Description Organize and plan clinical that is required for study sites and labs

Handle all international import and export documentation and shipping processes

Interface with managers and internal and external investors

Oversee shipping material supplies

Assume responsibility for set up and care of specimen collection kits

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