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- Clinical Research Coordinator
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November 12, 2010
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Deadline to register:
October 1, 2010
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Clinical Research Coordinating
Overview
Clinical Research is a method of testing used in the field of healthcare
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
- Associate of Applied Science Degree in
Clinical Research Coordinating
- Certificate of Completion in Clinical Research Coordinating
Late-start classes are available for this
program of study.
Employment Outlook*
Career opportunities for Clinical Research
Coordinators are found in hospitals, physicians'
offices, contract research organizations, biomedical
research organizations and institutions, specialty
disease centers and pharmaceutical and medical device
suppliers.
With the growth of the Biotechnology industry, Clinical Research
Coordinator positions are expected to increase by 2016.
On average, Clinical Research Coordinators earn an hourly rate of $27.03,
for an average annual salary of $56,216, or higher depending
on degrees obtained, the research setting, credentials and experience.
(According to Salary.com)
