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Job #02694

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) Washington 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 and prepare site visit reports (as required) 3) Participate in study development and start-up process, including reviewing protocols as well as designing and/or reviewing CRFs 4) Prepare informed consent forms and develop study documents 5) Organize and be present at investigator meetings 6) Work with the management on monitoring strategy and/or developing project-specific CRA training 7) Handle multiple projects and work both independently as well as in a team environment 8) Participate in clinical training programs and in maintaining awareness of developments in the field of clinical research (as needed) Requirements 1) BS/BA preferred 2) 1-year monitoring experience or a combination of on-site monitoring and clinical research coordination experience 3) In-depth knowledge of medical terminology and clinical monitoring process 4) Excellent therapeutic and protocol knowledge (as provided in company training) 5) Ability to handle customer service orientation 6) Excellent interpersonal and organizational skills 7) Superb attention to detail 8) Computer literacy and proficiency in MS Office 9) Excellent communication skills (verbal and written) 10) Willingness to travel – up to 65% (regionalized, depending on project needs)