Amanda Lesinski
BS
Ms. Lesinski is responsible for the oversight of the regulatory post activation for the 15 Treatment Modality Working Groups (TMWG) in the Clinical Trials Office at Winship Cancer Institute.
Titles and Roles
- Assistant Director, Regulatory Affairs, Post-Activation, Clinical Trials Office
- Winship Cancer Institute of Emory University
Biography
Amanda Lesinski, BS, is responsible for the oversight of the regulatory post activation for the 15 Treatment Modality Working Groups (TMWG) within Winship Cancer Institute Clinical Trials Office. 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.