Clinical Research Associate II - (Antioch, TN)

Essential responsibilities: Perform routine site monitoring visits, participate in site selection, site initiation, and study closure activities to ensure that the clinical trial is being conducted according to the approved protocol, amendments and in compliance with Good Clinical Practice (GCP) and all applicable regulatory qualifications. Duties and Responsibilities: Assist in the Investigator selection and qualification process Assist in the development of patient recruitment strategy Attendance at Investigator Meetings Perform and document pre-study site evaluations, site initiations, regulatory document collection, interim monitoring and study close out visits in accordance with GCP, study-specific qualifications, clinical monitoring plans, company standard operating procedures, applicable regulatory qualifications and defined quality and performance standards Ensure site IRB approval is current and all IRB documentation is in order