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
- CRCs
- Site Managers
- Principal Investigators
Karen L. Gilbert, B.S., C.C.R.A.
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$595
Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2.5 hours (0.25 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE#: 0778-0000-12-020-L01-P. Released: 4/12.
Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471