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

Try These Other Programs

CRA Training Programs At Universities | CROs | Professional Bodies