ACT — To determine which CITI training course(s) to take please answer the questions below as they apply to your research:
If more than one is applicable to you, please complete separately. Eg. If you are a human subjects researcher and you are a PI on a funded grant proposal, you will need to complete human subjects first and then reenter the system to complete the COI question also.
(IRB)
I conduct research involving human subjects or their data.
Required for all those who conduct research involving human subjects
(IACUC)
I conduct research, teaching or exhibition involving vertebrate animals.
Required for all those who work with vertebrate animals (e.g: animals with a backbone) in research, teaching, or exhibition, or those who oversee such work.
(RCR)
I am a student researcher (applicable to post docs also) being paid from a federal grant and need to complete Responsible Conduct of Research
training OR my college is requiring that I complete this training.
Required for all students and post docs being paid from a federal grant OR whose college requires this training.
(COI)
I am a Principal Investigator (PI), Co-PI or key personnel on a grant proposal submitted for funding through Sponsored Programs and need to complete Conflict of Interest training.
Required of all those key personnel who are included on grant proposals at FAU.
Additional training (Specialized)
I have already completed the required course training related to my area of study, but have been advised that there is additional training requirements that I did not originally anticipate. E.g. I am now doing research with Protected Health Information (PHI), I have recently begun working in a clinical trial or some other specialized area. Answer the questions below to determine which additional course applies to your research:
(HIPAA)
I obtain, use or disclose Protected Health Information
(PHI)
for research purposes.
(Good Clinical Practices - GCP)
I am or will be involved in an FDA regulated clinical trial of a drug, medical device, or biologic.
I have a role in managing, coordinating, or enrolling patients in a clinical trial.