IRB Researcher Training on eProtocol

This hands-on workshop provides researchers, study staff, and faculty with a comprehensive introduction to the eProtocol system for human subjects research. Participants will learn how to navigate the platform, create and submit new IRB applications, respond to reviewer requests, and manage post-approval activities throughout the life of a study. The session will cover key system features, required submission components, common application errors, and best practices for ensuring timely IRB review and regulatory compliance. Attendees will also receive guidance on submitting modifications, continuing reviews (when applicable), reportable events, and study closures. By the end of the workshop, participants will have the knowledge and confidence to effectively use eProtocol to support the ethical conduct and oversight of human subjects research.
Learning Objectives:

Navigate the eProtocol system and access research study records.
Create and submit new IRB applications and supporting documents.
Understand the IRB review workflow and how to respond to reviewer comments.
Submit modifications, reportable events, and study closures through the system.
Apply best practices to improve submission quality and minimize review delays.
Maintain compliance with institutional policies and human subjects research regulations.

Hosted by: Research Compliance