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.
Session topics include:
IRB Overview
Informed Consent
HRPP Committees
Conflict of Interest in Research
Budgeting, Policy on Documentation of Patient Participation, ICON Requirement and I-CART
Data Sharing
Division of Sponsored Programs
Research Billing
Biomedical Informatics Clinical Research Resources
Documentation
Data Security
Subject Safety
EPIC Tools for Clinical Research
ClinicalTrials.gov PRS