Attend sponsor/CRO monitoring visits (Pre-study, Initiation, Study-conduct, and closeout). - Attend/Complete Investigator Meetings, protocol training, company training, and industry conferences. - Coordinate monitoring visits. - Coordinate subject research visits. - Coordinate and/or perform delegated responsibilities for company-selected research protocols. - Collect, process, and ship research samples to a central lab vendor. - Pre-screening research subjects in the clinic database. - Manage study regulatory documents. - Coordinate company relationships with satellite sites ( Managing patients and protocol compliance). - Entering data into the site and sponsor clinical trial management system. - Reporting protocol deviations to sponsor and Institutional Review Board. - Submitting regulatory documents to the Institutional Review Board for study approval. - Providing study updates to the Investigators and company managers. - Recruiting research subjects from the clinic database and/or outside facilities. - Following the research protocol and reaching out to the sponsor/CRO about any concerns.
Locations
Altamonte Springs, FL • Clarkston, GA • Decatur, GA • Lithonia, GA • Lawrenceville, GA • Lilburn, GA • Marietta, GA • Norcross, GA • Roswell, GA • Smyrna, GA • Stone Mountain, GA • Tucker, GA • Conyers, GA • Duluth, GA • Kennesaw, GA • Waleska, GA • Fayetteville, GA • Griffin, GA • Jonesboro, GA • Morrow, GA • Forest Park, GA • Atlanta, GA • Gainesville, GA • Oakwood, GA • Athens, GA • Winder, GA • East Point, GA