Clinical Research Coordinator, On-Site, South Ogden, UT

Job description

Job Overview Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. Essential Functions: Provide clinical research support to investigators to prepare for and execute assigned research studies, including: - Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data - Attend all relevant study meetings - Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research - Recruit and screen patients for clinical trials and maintain subject screening logs - Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits - Design and maintain source documentation based on protocol requirements; - Schedule and execute study visits and perform study procedures - Collect, record and maintain research subject study...