The primary responsibility of the CRC is to manage all aspects of conducting clinical
trials. The CRC is the primary resource for the protocols and will act as liaison between
the investigators, primary care providers, the IRB and the sponsor. Along with the
investigator, the CRC will screen, enroll and follow study subjects, ensuring protocol
compliance and close monitoring while the subjects are on study. In addition, the CRC is
responsible for all data and source documentation, adverse experience reporting and
maintenance of complete regulatory files.
Where can I find a detailed job description for a Clinical Research Coordinator?
www.careercrusing.com
or google it
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