A new course entitled Clinical Research Coordinator (CRC)
is now available. The course provides a foundational training focusing on operational and regulatory elements necessary for the ethical conduct of clinical research, while at the same time it is specifically tailored to the needs of clinical research professionals. To supplement the CRC course organizations may also create an organization-specific module and learners may purchase Regulatory Binder Tabs to help organize information collected throughout the course of a clinical research study.
The CRC course is available to subscribing organizations for $500/year (unlimited number of learners), in addition to the base subscription fee, or to independent learners for $150/learner. It consists of 11 modules.
- CITI CRC Course: Overview
- Planning Research
- Funding, Financial Management, and Budgeting
- Working with the IRB
- Protocol Review and Approvals
- Principal Investigator (PI) Responsibilities
- Clinical Research Coordinator (CRC) Responsibilities
- Sponsor Responsibilities
- Informed Consent
- Site Management, Quality Assurance, and Public Information
- CRC Resources
CRC Organization-Specific Module
Organizations may supplement the CRC course with an organization-specific module. Requests made prior to 30 September 2015 will be included for no additional fee. Modifications to the module or requests made after this date are subject to CITI Program’s custom content development fees. Contact firstname.lastname@example.org
or get started on the CRC Module Questionnaire
to initiate the development of your organization's module.
Regulatory Binder Tabs
Regulatory Binder Tabs include brief information, instructions, definitions, and delineate between required and recommended information to retain throughout a study. Five additional site-specific tabs are also included for optional use. Visit our resources page
to download them at no additional charge.
How to Proceed