Issues with Human Subjects Research Data
Course Details
Course Objective
What happens when something goes wrong with human subjects research data? Is it an IRB or regulatory issue? What corrective actions need to happen, if any? When do I have to notify my participants?
Expert(s): Kim Serpico, MEd, CIP, Associate Director of IRB Operations, Office of Regulatory Affairs and Research Compliance, Harvard T.H. Chan School of Public Health
Host
Longwood Research Data Management Group
Target Audience
HMS Research Staff, Faculty, Postdocs, Grad Students
Course Duration
30 min.
Course Schedule
August 31, 2022, 12:00 pm to 12:30 pm