Audience
Health professionals working on human subjects research.
Objectives
Participants should be able to discuss the most current information and relevant approaches to research involving human subjects.
Purpose
To educate clinical research professionals on the basics of clinical research. There are also courses of interest on current and novel research. The lectures in this series will help provide a more effective, efficient and cohesive clinical research environment at the University of Iowa.
Fall 2025 Schedule
| Date | Time | Speaker | Title and Summary |
9/4/25
| Noon – 1:00 | Sandra Ahrendsen, BBA Senior Business Analyst, ICTS Michele Countryman, CIP Research Compliance IRB Director Shezad Gill, BS Clinical Trials Management Systems Analyst, ICTS Debra O’Connell-Moore, MBA Clinical Research Specialist, ICTS | Utilizing e-Reg for Signing Assurance Documents |
10/2/25
| Noon – 1:00 | Kim Sprenger, RN, BS Assistant Director, Clinical Research Support, ICTS Jackie Wangui, MSN, RN-BC Assistant Director, Clinical Research Resources, ICTS | Things to Consider When Developing a Budget & How to Interpret a Cost Analysis |
11/6/25
| Noon – 1:00 | Michele Countryman, CIP Research Compliance IRB Director Debra O’Connell-Moore, MBA Clinical Research Specialist, ICTS | Using 21CFR Part 11 Compliant DocuSign for Informed Consent |
Continuing Education Credit
The University of Iowa Carver College of Medicine
Each session in this educational series for a maximum of 1.0 AMA PRA Category 1 Credit(s) TM. Physicians should only claim credit commensurate with the extent of their participation in the activity.
The University of Iowa College of Nursing
Full time attendance for this program will award 1.0 contact hours.
Contact Information
If you have questions for presenters or suggestions for topics, please contact Dori Hinson