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Job #02696

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) San Diego, California Salary Highly competitive package, commensurate with experience Responsibilities 1) Monitor activities at clinical study sites to ensure adherence to Good Clinical Practices (GSPs), SOPs and study protocols 2) Review regulatory documents (as required) and prepare site visit reports 3) Participate in the study development and start-up process, including reviewing of protocols, designing and/or reviewing CRFs 4) Prepare informed consent forms, develop study documents 5) Organize and be present at investigator meetings 6) Work with management on monitoring strategy and/or developing project-specific CRA training (as required) 7) Handle multiple projects and work both independently as well as in a team environment 8) Participate in clinical training programs and maintain 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) Sound knowledge of medical terminology and clinical monitoring processes 4) In-depth therapeutic and protocol knowledge (provided in company training) 5) Excellent interpersonal and organizational skills 6) Good attention to details 7) Ability to provide customer service orientation 8) Computer literacy – proficiency in MS Office 9) Excellent verbal and written communication skills 10) Willingness to travel – up to 65% (regionalized, depending on project needs)