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Job #03047

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 Clinical Research Associate – East East Coast, USA Salary Highly competitive package, commensurate with experience Responsibilities 1) Manage 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) 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 experience including minimum 2 years of field monitoring experience within a CRO or other clinical research setting 3) Experience in oncology 4) Understanding of medical terminology, physiology and pathophysiology 5) Knowledge of Good Clinical Practices 6) Superb organizational skills 7) Ability to multi-task and work effectively in a fast-paced environment 8) Excellent communication (written and verbal) and diplomacy skills 9) Professional demeanor and appearance 10) Candidates from Midwest preferred 11) Willingness to travel (75% – 85%)