Clinical Research Coordinating
Overview
Clinical Research is a method of testing used in the field of health care
to gather safety and efficacy data for new drugs or medical devices.
Clinical Research Coordinating ensures good clinical practice guidelines are
followed throughout the testing process.
The responsibilities of a CRC include:
- Arranging for a research study site
- Recruiting, screening and enrolling clinical study participants
- Arranging follow-up visits
- Maintaining and dispensing drugs and other study supplies
- Completing and ensuring the accuracy of case report forms and regulatory documents
- Ensuring the adherence to good Clinical Practice guidelines.
CRCs work in a team environment under
the direction of Clinical Research Associates and principal investigators.
Program Certificate & Degree Options
Late-start classes are available for this
program of study.
Employment Outlook
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