Since 2016, the Institute for Clinical and Translational Science has been offering the Academy for Research Professionals three times a year to educate research coordinators and other staff about clinical research at the University of Iowa.

The workshop has been conducted both in-person and online, providing a basic framework of the roles and responsibilities of the research coordinator, the regulatory policy requirements for appropriate conduct of clinical research at the University of Iowa, and tools to assist coordinators to successfully perform their role. 

Academy for Research Professional Video Library

We have over a dozen available videos for ARP you can access.

Register for the Fall Academy Today!

Our Schedule:

Concept  

Topic  

Speaker 

Date 

Setting up a Study 

Study Start-Up/Orientation 

Debra O'Connell-Moore, MBA

9/18/25

  

  

 

Data Security Plan (DSP)  

Cait Flaherty, BA, JD

Emily Alward, BS, JD

9/25/25

Budgeting 

Kimberly Sprenger, RN, BS

 

  

  

 

IRB Overview (local submissions) 

Kelly O'Berry, BS, CIP

Rachel Kinker, MPA

10/2/25  

External IRB 

Mark Brunt, MBA, CIP

 

  

  

 

Human Research Protection Program (HRPP) Overview/Committee Intro 

Kelly O'Berry, BS, CIP

10/9/25

Research Billing Compliance 

Denise Krutzfeldt 

 

Conflict of Interest 

Christopher Taylor, MLIS, CAPM

Martha Hedberg, MPA

 

  

  

 

Unique forms/workflows 

Biosafety, Pathology, Pharmacy, MRPC, PRMC, and NRC

10/16/25

Clinical Research Unit 

Kimberly Sprenger, RN, BS

 

  

  

 

Data Sharing 

Brian Westra, MIS, MS, BA

10/23/25

Data/IT Security 

Kirk Corey, PhD

Gabby Perez, BS

Jordan Shebek 

 

  

  

  

 

Conducting a Study 

Biomedical Informatics/Data Governance 

Heath Davis, MS

Asher Hoberg, BS

10/30/25

Epic Tools (order sets and non-licensed order entry) 

Jillian Heisdorffer, CPhT, BA, BS-IT

 

  

  

 

Informed Consent 

Debra O'Connell-Moore, MBA

Kimberly Sprenger, RN, BS

11/6/25 

  

  

 

Advarra Clinical Trial Management System

Sandra Ahrendsen, BBA

Josiah Argo, BBA 

Shehzad Gill , BS

11/13/25

Biomedical Informatics (REDCap) 

Heath Davis, MS

Asher Hoberg, BS

 

  

  

 

Adverse Event/Serious Adverse Event identification and reportable events/reporting 

Debra O'Connell-Moore, MBA

Kimberly Sprenger, RN, BS

11/20/25 

Compliance (formerly PI oversight and documentation) 

Catherine Branham, MBA, CHRC

Alyssa Conrad, MS

Debra O'Connell-Moore, MBA

 

Documentation 

Debra O'Connell Moore, MBA

Kim Sprenger, RN, BS

 

  

  

 

Single IRB 

Michele Countryman, CIP

Mark Brunt, MBA, CIP

12/4/25