What is a Clinical Trials Monitor CRA
Monitors clinical trial sites for compliance, data integrity, and participant safety | conducts site visits and source data verification to ensure trial quality.
Clinical Trials Monitor CRA Core Duties
Conduct Site Initiation | Monitoring | Closeout Visits | Perform Source Data Verification And Regulatory Document Review | Ensure Protocol Adherence And Safety Reporting | Prepare Monitoring Reports And Follow Up On Corrective Actions.
Clinical Trials Monitor CRA Education Requirements
Bachelor Degree In Life Sciences Or Nursing With GCP Training
Clinical Trials Monitor CRA License and Accreditation Agency
ACRP | SOCRA Related Credential
Clinical Trials Monitor CRA Program Length
6 to 36 Months
Clinical Trials Monitor CRA Salary Min and Max
$60000 to $130000
Clinical Trials Monitor CRA Work Settings
CROs | Pharma Companies | Academic Research Organizations
Clinical Trials Monitor CRA Key Skills
Site Monitoring | SDV | Regulatory Review | Monitoring Report Writing
Look for These Programs
CRA Training Programs At Universities | CROs | Professional Bodies