VOIANT℠
Laura Guzman has over 19 years of work experience in various roles related to quality assurance, regulatory compliance, project management, and research. Their most recent position was as the VP of QA & Regulatory Compliance at VOIANT™, starting in September 2023. Prior to that, they worked at MedQIA, starting as a Research Technologist in 2004 and progressing to roles such as QA Manager and Director of Quality. Laura also gained experience at UCLA Health as a Project Manager and Administrative/Project Assistant. Overall, Laura has a strong background in ensuring quality and regulatory compliance within organizations.
Laura Guzman completed their Bachelor of Science in Biology from Universidad de Antioquia between 1997 and 2002. Laura later pursued their Master of Arts from Northwestern University, specializing in an unspecified field of study, from 2005 to 2007. Lastly, they obtained a Master of Science in Regulatory Science from the University of Southern California between 2011 and 2015.
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VOIANT℠
Three industry leading companies, MedQIA, WorldCare Clinical and DARC, have come together to form Voiant, the new leader in clinical trial imaging endpoint data. We are the industry leading AI-based clinical trial imaging solution with unparalleled scientific and clinical domain expertise, providing biopharmaceutical companies with high-speed delivery of quality clinical endpoint data. We combine leadership in artificial intelligence and visionary computing, key opinion leaders for strategic therapeutic areas alignment and clinical research experts to deliver operational excellence and consistent execution - providing the shortest path to the highest quality imaging data for clinical trials.