Clinical Research Coordinator

Aurora, CO or Colorado Springs, CO, United States (On-site) | Full-time | Clinical Trials experience is a must. DESCRIPTION: Coordinates clinical research program by identifying and assessing patients, distributing information, acting as a clinical resource for the study physicians, sponsor representatives, and patients, conducting follow-up care for patients, and attending meetings pertaining to the clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following Conducts clinical research studies according to study sponsor requirements in conjunction with FDA and ICH/GCPs guidelines. Conduct clinical research studies according to the designated pharmaceutical sponsor’s protocol. Provide documentation of all study procedures conducted in a clinical trial. Recruit and maintain patients in assigned studies. Perform necessary protocol-related procedures. Screen potential patients both via phone and in the office. Keep investigators updated on the patient’s status and any changes in the patient’s medical condition that the patient has not reported to the doctor. #J-18808-Ljbffr