The Clinical Research Coordinator III identifies, analyzes and interprets research participant and/or trial information and uses sound knowledge, skill and judgment to respond proactively and/or in a timely manner.
Clinical Research Analyst is responsible for the coordination of Clinical trials, from protocol review and ethics approval, through to trial closure. Main responsibilities include recruitment and tracking of study participants (e.g. obtain informed consent, and administer questionnaires).
Educates nursing, pharmacy and clerical staff about new protocols or amendment implementation and their roles in the implementation; assists investigators in the proper conduct of all research protocols being conducted by the department in accordance with departmental policy, institutional policy, sponsor/protocol requirements and FDA regulations.