Summarized Purpose: Clinical Research Coordinator/Nurse Coordinator with minimum one year experience in the role. Conducts multiple ongoing clinical trials involving patients or healthy volunteers/subjects. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, and retention of study participants. Required experience with EDC, IRT system. Should be able to independently conduct subject visits in a clinical trial.
Essential Functions: