Orientation for New Clinical Research Coordinators

This workshop is strongly recommended for all clinical research coordinators (CRC’s) who are new to the research role or new to working at UNC. The intent is to introduce new CRC's to the UNC offices involved in clinical trials, the federal and local regulations governing conduct, and provide an overview of best practices utilized in the implementation of clinical research.

When May 18, 2012
from 08:30 AM to 12:30 PM
Where Brinkhous-Bullitt, Room 219
Contact Name
Contact Phone 919.966.6844
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Pre-requisites for attending this workshop are completion of the CITI Good Clinical Practice (GCP) and CITI Ethics online courses available at: https://www.citiprogram.org/Default.asp.

The objectives of this workshop are to:

• Review human subject research protection and the IRB

• Discuss research compliance and required approvals at UNC

• Review use of the Clinical Research Management System (CRMS)

• Review basic elements of contract negotiation and grant management

• Define appropriate responsibilities for study team members

• Describe steps for successful implementation of a study

• Describe appropriate management of study documentation

• Define Good Clinical Practices (GCP)

• Review the informed consent process

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