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Job #02926

About our client Our client is an international CRO that provides full-service clinical trials management support for various therapeutic areas, such as oncology, cardiology and medical devices. Their vision is to become the preferred CRO for life science companies across the world. This is a great opportunity for someone looking for growth and an exciting challenge! Position Location CRA – Permanent Colorado Salary Highly competitive package, commensurate with experience Responsibilities 1) Manage (with minimal supervision) the implementation and conduct of study protocols at research sites 2) Perform monitoring visits, including site qualification, initiation, monitoring and closeout visits while maintaining regular contact with study site 3) Ensure protocol/GCP compliance 4) Participate in Investigator meetings and other study training meetings (as required) 5) Prepare for and participate in sponsor and FDA audits 6) Mentor junior staff Requirements 1) BS/BA in a medical/scientific discipline (or equivalent combination of education and experience) 2) 3+ years of experience with minimum 2 years in field monitoring (in a CRO or other clinical research setting) 3) Good understanding of medical terminology, physiology and pathophysiology 4) Working knowledge of GCPs 5) Excellent organizational skills 6) Ability to multi-task and work effectively in a fast-paced environment 7) Superb diplomatic and communication (written and verbal) skills 8) Professional demeanor and appearance 9) Willingness to travel (75% – 85%)