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Job #02693

About our client Our client is a global CRO headquartered in New York. They focus on the development of therapeutics for oncology and dermatology. The company has an experienced management team, a robust pipeline and an empowering corporate culture that is focused on the professional development of its employees. Position Location Regional CRA (Home-Based) Colorado Salary Highly competitive package, commensurate with experience Responsibilities 1) Manage the implementation and conduct of study protocols at research sites with minimal supervision 2) Perform monitoring visits, including site qualification, initiation, monitoring and closeout visits 3) Maintain regular contact with study site to 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 or equivalent combination of education and experience in a medical or scientific discipline 2) 3+ years of experience and minimum 2 years of field monitoring expertise in a CRO or other clinical research setting 3) In-depth understanding of medical terminology, physiology and pathophysiology 4) Working knowledge of Good Clinical Practices (GCPs) 5) Excellent organizational skills 6) Ability to multi-task and work effectively in a fast-paced environment 7) Professional demeanor and appearance 8) Excellent communication (written and verbal) and diplomatic skills 9) Willingess to travel (75% – 85%)