OHRP
Rockville, MD
Ms. Sly has supported clinical trials in the fields of Institutional Review Board (IRB) administration, clinical trial site start-up and regulatory support for over 15 years. She currently holds the position of Compliance Program Analyst with the Office of Human Research Protections (OHRP). Previously she served as the Director of the National Cancer Institute's Central Institutional Review Board (NCI CIRB) and has throughout her career served both local and central IRBs providing analysis and review of all categories of research including exempt, expedited and full board level research proposals in both biomedical and social/behavioral research. In addition, she is responsible for supervising other IRB Coordinators, managing workflows and implementing process improvement strategies within the IRB management offices.
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B06 - Essential Documentation: IRB Record Keeping, Written Procedures, Minutes, and More
Wednesday, November 17, 2021
1:45 PM – 2:45 PM ET