Beth Bieze, MA, CCRA, ACRP-PM, FACRP

Clinical Quality Management Director

ProTrials Research Inc.

Beth Bieze, MA, CCRA, ACRP-PM, FACRP, has over 20 years of experience in the Clinical Research field, starting as a Clinical Trial Assistant and advancing through roles such as CRA, Lead CRA, Project Manager, Associate Director/Trainer, and Director of Clinical Quality Management. Her expertise has been shaped primarily within CRO environments, with significant involvement in the Functional Service Provider (FSP) model. she has extensive experience across multiple therapeutic areas and indications, which has allowed me to develop a deep understanding of diverse clinical research landscapes. Her contributions to bids and proposals and ensuring that new studies are thoroughly prepared for success have been key aspects of my career. Her leadership extends to ensuring strict adherence to regulatory requirements, GCP standards, and fostering a culture of quality and compliance. A significant aspect of her role involves mentoring and being a resource to my team, addressing inquiries on a wide range of topics - which she loves.

Session

• Workshop—Project Management Basics for Clinical Research