CRNC is responsible for coordinating the research activities of IRB-approved study protocols. Specific protocols that require the CRNCs support will be determined by the Department Head of Clinical Investigation Department (CID) in consultation with the Clinical Research Coordinator.
Coordinate and manage a variety of activities involved in operating the simulation and clinical lab. Participate in the development, coordination and implementation of simulator training for healthcare professionals and students.
In this role, you will be responsible to performs research; analysis; development and evaluation of systems; procedures and models in assigned functional area. Analyzes and defines problems and researches possible solutions that afford maximum probability for profit or effectiveness in relation to cost or risk.
In this role, you will be responsible for coordinating the research activities of assigned IRB-approved study protocols Reports and is responsible to the Principal Investigator (PI) and supports the CID department head in accordance with federal and local regulatory guidelines.