Archive: CRC Role/Responsibilities Training

April 24, 2012 | Barnett International Recording

Web Seminar Archives are available in either USB Flash Drive or DVD Format.

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.

*
*
$625.00

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

Instructor

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.