Biography
Amanda Lesinski, BS, is responsible for the oversight of the regulatory post activation for the 15 Treatment Modality Working Groups (TMWGs) for the Clinical Trials Office at Winship Cancer Institute. Ms. Lesinski joined the CTO with over 16 years of experience in clinical trials research. Prior to joining Winship, she served as a clinical trials auditor with an NCI-designated comprehensive cancer center where she gained knowledge and expertise in auditing, clinical trials oversight, and FDA inspections. Ms. Lesinski has additionally functioned as a clinical trials quality assurance consultant.
Education
Ms. Lesinski received her bachelor's degree in Biology Sciences from Bowling Green State University in Ohio.
Titles & Roles
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Assistant Director, Regulatory Affairs, Post-Activation, Clinical Trials OfficeWinship Cancer Institute of Emory University