Clinical Research Coordinator I

The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases. The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures. The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols. The Clinical Research Coordinator is also responsible for keeping all data and source documentations, adverse event reporting, and IRB regulatory files.
• Must be able to interact well with patients and the general public Ability to acquire and maintain all required CITI training certificates Ability to acquire and maintain credentialing at all required institutionsClinical Research Coordinator I (Pay Grade 23) Bachelor's degree or RN with current state licensure at the time of hire OR LPN with current state licensure at the time of hire and three (3) years of related work experience Level I Expressed interest in Clinical Research Motivated to learn about Clinical Research and associated regulations