Amanda S.

Amanda S. has over 18 years of experience in clinical research and regulatory affairs. Currently employed as a Sr. Manager for Quality & Regulatory at DaVita Clinical Research since December 2020, Amanda previously held the position of Associate Project Manager at IQVIA Biotech from June 2019 to December 2020. Amanda's extensive career includes roles as a Clinical Research Coordinator and Quality Assurance Specialist at eStudySite, a Research Administrator at UNIVERSITY CLINICAL RESEARCH, and QA Associate/QC Specialist at PROFIL INSTITUTE FOR CLINICAL RESEARCH. Prior positions include Sr. Clinical Trials Associate at QUINTILES, Regulatory Specialist II at Covance CRU, Inc., IRB Coordinator/IRB Operations Assistant at Aspire IRB, LLC, and Study Manager/IRB Coordinator at Biomed IRB.