Event Description
The Office of Research & Innovation (ORI) is offering a Clinical Research Training Series from March through September 2025, featuring interactive sessions on key topics, including:
•Regulatory administration
•Informed consent processes and procedures
•Investigator obligations
•Root cause analysis and event reporting
•Protocol compliance and how to avoid common challenges
The first and last sessions will be held in person, while all others will be conducted remotely for your convenience. There is no cost to participate, but space is limited — register here today!
Who should attend?
This series is designed for all students, staff, and faculty who conduct interventional studies, observational studies, or behavioral and public health research. Whether you're new to clinical research or looking to enhance your skills, this series will incorporate the newly released ORI Clinical Research Guidelines and Tools to support best practices.
Planned Cohort Series
1. March 3rd, 2025 from 1:00-3:00pm: Informed Consent Process & Documentation (In Person)
2. April 9th, 2025 from 11:00-12:30pm: Regulatory Administration (Virtual)
3. May 14th, 2025 from 11:00-12:00pm: Training and Qualification (Virtual)
4. July 9th, 2025 from 11:00-12:00pm: Protocol Compliance (Virtual)
5. August 13th, 2025 11:00-12:30pm: Participant Protection, Adverse Events, and Reporting (Virtual)
6. September (TBD-Week of September 15th): Common Audit Findings and Root Cause Analysis (In Person)
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