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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