Tabitha Artz

Tabitha Artz has extensive experience in clinical affairs and regulatory affairs, primarily at the Sarah Cannon Research Institute since September 2010. As Manager of Clinical Affairs, Tabitha leads a team, manages regulatory documentation, and oversees compliance with FDA and GCP standards. Tabitha's career progression at Sarah Cannon includes roles as Senior Clinical Research Associate and Lead Regulatory Affairs Specialist, where responsibilities included training staff, managing IRB submissions, and ensuring adherence to SOPs. Prior to this, Tabitha worked as Administrative Manager and Senior Project Manager at Seaboard Health Care Search, where expertise in physician placement was developed. Tabitha's educational background includes a Bachelor's degree in Journalism from Middle Tennessee State University and legal studies at The University of Memphis—Cecil C. Humphreys School of Law.