To apply for multiple jobs at once, please select the check box beside the desired jobs on the main job category page.

Job #02708

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) Dallas, Texas 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) Oversee multiple projects as well as work both independently and in a team environment 4) Participate in study development and start-up processes 5) Handle reviewing of protocols, designing and/or reviewing of CRFs, preparing of Informed Consent Forms (ICFs) and developing of study documents 6) Organize and remain present at investigator meetings 7) Work with the management on monitoring strategy and/or developing project-specific CRA training 8) 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 a combination of on-site monitoring and clinical research coordination experience 3) Superb knowledge of medical terminology and clinical monitoring processes 4) In-depth therapeutic and protocol knowledge (as provided in company training) 5) Computer literacy (proficiency in MS Office) 6) Ability to provide customer service orientation 7) Excellent interpersonal and organizational skills with superb attention to detail 8) Excellent verbal and written communication skills 9) Willingness to travel – up to 65% (depending on project needs)