Content Contributor Belinda Smith

Belinda Smith, MS, RD, CCRC

University of Kentucky Office of Research integrity

Belinda Smith is a research education specialist with 34 years of experience, beginning in clinical research coordination and evolving into human subject protections. She currently oversees education and outreach for the University of Kentucky Human Research Protection Program and provides FDA consultation for the Office of Research Integrity and IRBs. She has co-authored publications and presented nationally in the areas of metabolic research and human research protection. The UK Informed Consent Workshop received the 2018 Human Research Protection Award of Excellence for Best Practice and in 2020, the UK Education Program was recognized by AAHRPP as an Area of Distinction.

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Biomedical (Biomed) Comprehensive

CME/CEUFeatured

This course provides an expansive review of human subjects research topics for biomedical researchers.

Biomedical (Biomed) Comprehensive

IRB – Biomedical Focus

CME/CEUNew

Provides foundational training for IRB members involved in the review of biomedical human subjects research.

IRB – Biomedical Focus

IRB – Social-Behavioral-Educational Focus

CME/CEU

Provides foundational training for IRB members involved in review of social-behavioral-educational human subjects research.

IRB – Social-Behavioral-Educational Focus

IRB – Biomedical and Social-Behavioral-Educational Combined

CME/CEU

Provides foundational training for IRB members involved in the review of both biomedical and social-behavioral-educational huma...

IRB – Biomedical and Social-Behavioral-Educational Combined

Remote Informed Consent: The Same, but Different, but Still the Same

New

Presents remote consent considerations and scenarios.

Remote Informed Consent: The Same, but Different, but Still the Same