Summit: Principal Investigator Responsibilities

Practical information on the fundamentals of being a principal investigator (PI).

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About this Course

The course is designed for clinicians seeking to enter the field of clinical research. It provides guidance on topics such as Form FDA 1572s, financial disclosure forms, selecting and training staff, delegating tasks, and maintaining oversight. It offers instruction on serious adverse events, monitoring visits, audits, and inspections.

Language Availability: English

Suggested Audiences: Clinicians, Faculty, Investigators, Postdocs, Research Administrators, 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: Principal Investigator Responsibilities

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): 21550 (English)


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