Checkout 0
Training Courses - Web Seminar Archives

Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.

Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).

Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.

Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.

Archive: CRC Role/Responsibilities Training

Course #: BI10837
April 24, 2012

Course Description

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.

Video Preview


Learning Objectives

  • 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

Who Should Attend

  • CRCs
  • Site Managers
  • Principal Investigators


The course will be led by one of the following instructors:

Karen L. Gilbert, B.S., C.C.R.A.

Click here for complete trainer biographies


Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.