CLINICAL RESEARCH COORDINATOR (CRC)
The CRC series provides a foundational training specifically focused on operational and regulatory elements necessary for the ethical conduct of clinical research, while at the same time tailored to the needs of clinical research professionals. It offers learners a foundation that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) training.
Organizations may supplement the CRC course with an organization-specific module. Contact firstname.lastname@example.org or get started on the CRC Module Questionnaire to initiate the development of your organization's module.
For a listing, description, language availability, and recommended use of each module in the CRC series, download the CRC Catalog (PDF file).
For recommendations on using this series, download Using CITI Program Content: Clinical Research Coordinator (PDF file).
CRC content is intended for CRCs, investigators, and other clinical research professionals. It is also useful to those pursuing a career in clinical research. The basic CRC course is intended as foundational role-based training for learners needing basic CRC training or organizations needing on-boarding training for new CRCs.
Pricing and Subscription Options
Available to subscribing organizations starting at $500 USD/year, which is in addition to the base subscription. Independent Learner registration is available for $150 USD.
- Subscribe as a new organization.
- Subscribe as an existing organization.
- Register as an Independent Learner.