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