Summit: Coordinating Clinical Trials

Hands-on instruction on day-to-day practices of clinical research coordinators (CRCs).

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About this Course

The course provides information on specific areas such as applying inclusion/exclusion criteria, taking vital signs, recording a medical history, managing subject visit flow, completing source documentation and electronic data capture, and communicating with sponsors and contract research organizations. The content is ideal for onboarding new clinical research coordinators (CRCs) and introducing them to the core practices of coordinating clinical research.

Language Availability: English

Suggested Audiences: Clinical Research Coordinators (CRCs), Investigators, Nurses, Research Administrators, Research Assistants, Students, Study Sites

Organizational Subscription Price: Included as part of an annual subscription to our Summit: PI and CRC Responsibilities series, available for $675 per year/per site as a subscription add-on for government and non-profit organizations; $750 per year/per site as a subscription add-on for for-profit organizations
Independent Learner Price: $99.39 per person


Course Content

Summit: Coordinating Clinical Trials

By the end of this course, you should be able to:

  • Describe the process for screening and enrolling subjects into a clinical trial.
  • Discuss best practices for managing participant visits.
  • Explain how to reference a protocol, document deviations, and report adverse events.
  • Detail how to create and maintain source documentation.

Recommended Use: Required
ID (Language): 21540 (English)


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