Begin a career in the rapidly expanding clinical research industry. In this eleventh session of the series, we will examine the role of the Clinical Research Associate and others in ensuring high quality data in clinical trials through monitoring, quality assurance, and audits.
Upon completion of this course, you will be able to: describe the purpose and process for monitoring study data; describe the role of the clinical research associate (CRA), clinical study coordinator, and investigator during a monitoring visit; discuss monitoring in the context of data integrity, including source document verification; and, extrapolate specific operational and safety risks that could occur if data quality issues are identified or if inadequate monitoring is conducted.
Attend only the sessions that interest you most, or register for all 12 sessions for the price of 10. Attend 10 sessions to receive a Professional Certificate of Completion in Clinical Research Foundations.