Sept. 20 - Navigating Investigator Initiated Human Subjects Research (Without a Sponsor’ Safety Net)

Can't attend in person? Here is a Zoom link.

Hybrid workshop: "Navigating Investigator Initiated Human Subjects Research (Without a Sponsor' Safety Net)

This panel discussion will touch on diverse areas supporting human subject research. Panelists will include representatives from the Human Subjects Protection Program office (covering clinicaltrials.gov, iRIS, compliance, etc.), the IRB, local health care facilities, the UofL Privacy Office, UofL Legal, UofL Libraries, and more. You’ll walk away with details about how these offices support the efforts of researchers, regulatory staff, and clinical support staff. Time will be reserved for you to consult one-on-one with the IRB chairs and all HSPPO staff, along with the panelists and their co-workers.

Panelists include:

Laura Clark, M.D., IRB Chair

Julie Goldman, M.D., IRB Vice Chair

Matthew Hawthorne, J.D., Norton Research

Misty Hooper, CPA, UofL Health

Mechelle Kaufman, RN, HSPPO

Rachel Keith, Ph.D., Environmental Health Institute

Sarah King, Norton Healthcare

Dani LaPreze, MLS, Kornhauser Library

Stacie McCutcheon, MA, CHPC, CCEP, UofL Privacy Officer

Shannon Pipes, J.D., University Senior Counsel; and a representative from Norton Healthcare’s research office.

Paula Radmacher, Ph.D., IRB Vice Chair

Haylee Ralston, J.D., EVPRI

Phil Rosenbloom, M.D., Ph.D., IRB Vice Chair

Rachel Shepherd, MBA, Clinical Trials Unit

Moderated by Christy LaDuke, CIP, HSPPO.