Training (HRPP)
All study personnel who are listed on an IRB study, interact with human research participants, participate in an intervention with human research participants, or who access private, identifiable information about participants must complete required training through the Collaborative Institutional Training Initiative (CITI).
CITI Human Subjects Research Training Course is a self-paced web-based training covering core ethical concepts and regulatory requirements. Purdue University requires all individuals engaged in the conduct of human subject research to have current CITI certification, which must be updated by a refresher course after 4 years.
The CITI Human Subjects Research Basic Course is required for all investigators and study personnel (i.e., Users) who have not previously completed a CITI human subjects research course. You do not need to complete the entire Course in one session. Re-enter as often as you like, using your username and password, to complete the training.
At a minimum, you must complete one of the following in CITI:
- Biomedical Research for Investigators and Key Personnel Learner Group
- Social Behavioral Research for Investigators and Key Personnel Learner Group
- Use this CITI Registration Instruction Sheet to assist you in registering with CITI.
You must complete all required modules with a cumulative score of 80% or better to pass the course.
Researchers conducting clinical trials are required to complete Good Clinical Practice (GCP) training. GCP training is available through the CITI Program.
- NIH requires GCP-trained personnel to complete a refresher course every 3 years
- Principal Investigators are responsible for ensuring all team members maintain current GCP credentials
See the Clinical Trials page for more information on GCP requirements.
CITI Program offers many recorded webinars on a range of topics of interest to Purdue researchers engaged in human subject research. These are available at:
CITI All-Access Webinar Package
Please see our quick reference guide for help accessing the webinars.
Short videos demonstrating specific PERA steps on topics such as Create a New Study, Study Modifications, Responding to Clarifications and many other PERA activities.
Written Instructions on different topics such as Create a new Study, Study Modification, Responding to Clarifications and many other PERA activities.
The Office of Human Research Protections (OHRP), within the U.S. Department of Health and Human Services (HHS), offers a variety of free online trainings for the research community on human research protections based on the principles of the Belmont Report and the requirements of the revised Common Rule (or 2018 Requirements).
We also offer group training and presentations for classes and other groups at Purdue. Please use the link below to request group training.
† Requires Purdue career account authentication
Investigators are responsible for knowing the training requirements associated with their study protocols and maintaining records for verification.