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Job #02743

About our client Our client is a world-leading CRO, which has served the pharmaceutical, biotech and healthcare industries for over 25 years. Position Location Regional Clinical Research Associate (Office/Home-Based) Utah 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) Handle multiple projects, both independently and in a team environment 4) Participate in the study development and start-up process, including reviewing protocols, designing and/or reviewing CRFs, preparing informed consent forms, developing study documents 5) Organize and remain present at investigator meetings 6) Work with the management on monitoring strategy and/or developing project-specific CRA training 7) Participate in clinical training programs and maintain awareness of developments in the field of clinical research (as needed) Requirements 1) BS/BA 2) 1-year monitoring experience or combination of on-site monitoring and clinical research coordinator experience 3) Experience in oncology preferred 4) Sound knowledge of medical terminology and clinical monitoring process 5) In-depth therapeutic and protocol knowledge (as provided in company training) 6) Ability to provide customer service orientation 7) Computer literacy (proficiency in MS Office) 8) Excellent interpersonal and organizational skills 9) Superb attention to detail 10) Excellent communication (verbal and written) skills 11) Willingness to travel – up to 65% (depending on project needs)