Training
Human Subjects Protection Training
Training should be completed as part of the application process for new studies and/or for any new involvement in research. The courses listed below are currently accessible through the CITI Program.
Follow these directions to affiliate with UTRGV on the CITI Program site (new users)
For Expedited and Full Review studies, all research team members must complete or have a current training course for Human Subjects Protection and Responsible Conduct of Research. Both of these courses are good for 4 years.
Please note, Tick@Lab has a CITI Integration function which allows staff to verify completed training courses without the need for researchers to submit reports.
Note: Choose one course, selection depends on the type of research you will be involved in.
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Social-Behavioral-Educational Basic
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Biomedical (Biomed) Basic
Choose one course, selection depends on the type of research you will be involved in.
- Biomedical Responsible Conduct of Research Course
- Social Behavioral Responsible Conduct of Research Course
Clinical Research
If you will be conducting a clinical trial or clinical research, please complete the applicable course(s) below for Good Clinical Practice in addition to the above-mentioned courses.
- Good Clinical Practice Social and Behavioral Research Best Practices for Clinical Research
- Good Clinical Practice for Clinical Investigations of Devices
- Good Clinical Practice for Clinical Trials with Investigational Drugs and Biologics (ICH Focus)
- Good Clinical Practice for Clinical Trials with Investigational Drugs and Medical Devices (U.S. FDA Focus)
NOTE: Selection depends on the type of clinical research you will conduct or be involved in.