The Clinical Research Coordinator (CRC) can be a key liaison between the investigator, subject, Institutional Review Board (IRB), and sponsor. The CRC assists the investigator to ensure that the clinical trial is successfully implemented and completed. This web seminar presents the core skills and activities performed by the CRC and the documentation requirements that come along with clinical trials.
- Define the role of the CRC at the research site
- Identify appropriate delegation of study tasks to CRCs
- Identify required subject and non-subject documentation requirements
- Identify key activities performed by the CRC monitored by the sponsor
- Site Managers
- Principal Investigators
The course will be led by one of the following instructors:
Karen L. Gilbert, B.S., C.C.R.A.
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Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.