임상시험의 모니터링을 담당하기 위해 의뢰자에게 지정한 자

Peron employed by the sponsor or CRO who is responsible for determining that a trial is being conducted in accordance with the protocol. NOTE : A monitor’s duties may include, but are not limited to, helping to plan and initiate a trial, assessing the conduct of trials, and assisting in data analysis, interpretation, and extrapolation. Monitors work with the clinical research coordinator to check all data and documentation frm the trial.