The Importance of Clinical Trial Master Files (TMF) with Doran Triggs, BS

SCCR’s Quality and Compliance Manager, Doran Triggs, BS, provides an overview of the trial master file (TMF) and importance of maintaining a TMF. At the conclusion of this class, you will be able to: • Understand the definition of TMF and ISF • Recognize the requirements • Learn how to manage the TMF • Identify recommended contents for TMF • Understand Inspection Readiness • Outline common errors About the Speaker: Doran Triggs, BS, is a Clinical Research Coordinator II, within SCCR’s Quality and Compliance team. Doran has been in the clinical research field for over four years. She first joined SCCR in 2018 as a CRC working on Vascular Surgery and Women's Heart Health trials. Within her four years, Doran focused her training on regulatory compliance and study data monitoring. Since 2021 she has transitioned to a role on SCCR's Quality and Compliance team where she provides support to study teams within SCCR. Most recently she helped develop and manage SCCR's monitoring program as well as monitor multiple trials within SCCR and other departments across Stanford University School of Medicine.