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Job #02872

About our client Our client is a global CRO that serves the pharmaceutical, biotechnology and medical device industries. The company is built upon a strong foundation of clinical, process and systems expertise. They specialize in major therapeutic areas such as oncology and dermatology. Position Location Regional Clinical Research Associate (Home-Based) Midwest, USA 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 3) Maintain regular contact with study site to ensure protocol/GCP compliance 4) Prepare for and participate in sponsor and FDA audits 5) Participate in Investigator meetings and other study training meetings (as required) 6) Mentor the junior staff Requirements 1) BS/BA in a scientific or medical discipline (or equivalent combination of education and relevant experience) 2) 3+ years of experience in oncology 3) Minimum 2 years in field monitoring (within a CRO or any other clinical research setting) 4) Knowledge of medical terminology, physiology and pathophysiology 5) Working knowledge of GCPs 6) Excellent organizational skills 7) Ability to multi-task and work effectively in a fast-paced environment 8) Superb communication skills (written and verbal) 9) Professional demeanor and appearance along with ability to be diplomatic 10) Willingness to travel (75% – 85%)