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Job #02705

About our client Our client is a world-leading CRO, which has served the pharmaceutical, bio-tech and healthcare industries for over 25 years. Position Location Regional Clinical Research Associate (Office/Home-Based) Nevada Salary Highly competitive package, commensurate with experience Responsibilities 1) Monitor activities at clinical study sites to ensure adherence to Good Clinical Practices (GCPs), SOPs and study protocols 2) Review regulatory documents (as required) and prepare site-visit reports 3) Participate in clinical training programs and maintain awareness of developments in the field of clinical research (as needed) 4) Handle multiple projects and work both independently as well as in a team environment 5) Participate in study development and start-up processes 6) Handle reviewing of protocols, designing and/or reviewing CRFs, preparing Informed Consent Forms (ICFs) and developing study documents 7) Organize and remain present at investigator meetings 8) Work with the management on monitoring strategy and/or developing project-specific CRA training Requirements 1) BS/BA 2) 1-year monitoring experience or combination of on-site monitoring and clinical research coordination experience 3) In-depth knowledge of medical terminology and clinical monitoring process 4) Experience in oncology preferred 5) Superb therapeutic and protocol knowledge (as provided in company training) 6) Computer literacy (proficiency in MS Office) 7) Excellent interpersonal and organizational skills as well as keen attention to detail 8) Excellent communication (verbal and written) skills 9) Willingness to travel – up to 65%