What are the responsibilities and job description for the Clinical Research Coordinator (LVN/RN) - Research position at Diagnostic Clinic?
Description
Primary responsibilities include coordinating, implementing, managing and completing clinical research trials. This is done by recruiting and screening study participants, obtaining informed consent or parental permission / assent, educating research subjects or parents of participants, scheduling and conducting study visits and procedures, collecting and recording study data, maintaining study records, interfacing with study sponsors, study monitors, study doctors and study team and knowing and adhering to the study protocol.
Requirements
Candidate will possess experience working in a medical environment and have an RN or LVN license (preferred). Clinical research trial experience is a plus, but not mandatory. Must have above average skills in computer use with various types of software; demonstrate ability to coordinate and establish priorities among diverse tasks; effectively communicate verbally and in writing. Must be able to work independently and be self-motivated. Needs to be able to think critically, excel in project management, organize, and coordinate multiple clinical trials.
