Job Description Summary
-Monitors patient data & study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely and accurate monitoring of patient data and study-related information from source documents research records and site visits where applicable. May monitor study sites and audit facility selection.Job Description
Major Accountabilities
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Skills Desired
Clinical Monitoring Clinical Research Clinical Study Reports Clinical Trial Management Systems Clinical Trials Collaboration Data Integrity Decision Making Skills LifesciencesRequired Experience:
IC
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