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[email protected] (619) 594-6622
Human Research Protection Program Staff
Administrative Analyst
Justin Dean
[email protected]
Location: Gateway Center 4th Floor
IRB Regulatory Compliance Analysts
Lead IRB Compliance Analyst
Anne Dodge-Schwanz
[email protected]
(619) 594-1448
IRB Compliance Training Specialist
Eric Morgan
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(619) 594-4057
Eric provides overall guidance and direction for ClinicalTrials.gov related reporting for human subjects’ research that involve clinical trials. This includes establishing user accounts for research investigators in the ClinicalTrials.gov Protocol Registration System (PRS). Updating clinical trial study records so that study information is current and accurate.