8 MAY 2025TECH OUTLOOKIN MY OPINIONCHARTING A TRAILBLAZING PATH IN CLINICAL DEVELOPMENTBy Maribelle Guloy, Director of Clinical Development, American Regent, IncMaribelle Guloy is the Director of Clinical Development at American Regent, a company of Daiichi Sankyo. Before joining American Regent, Dr. Guloy held various full-time and consulting roles at CROs, pharmaceutical, and biotech companies, including Moderna.Dr. Guloy is an active member of the professional community. She serves on the Advisory Board of the University of California, Irvine (UCI) Clinical Trials, Medical Device, and Drug Development program and UCI's Beall Innovation program. She has also served on the Board of Directors for the Society of Clinical Research Associates, Inc.Dr. Guloy earned her Doctor of Health Science in Global Health from Nova Southeastern University in Florida, her Master of Science in Health Science and Clinical Research Administration from George Washington University in Washington, DC, and her Bachelor of Science in Medical Technology from the University of Immaculate Conception in the Philippines.From Milestones to MasteryMy journey in clinical development began in 2000 when I co-founded and managed an oncology-focused clinical research organization (CRO) for 16 years. Working in a smaller company provided me with the flexibility and opportunity to pursue my master's and doctoral degrees, with a vision to transition into the clinical science and drug research & development space.In 2007, I joined the University of California Irvine's (UCI) Life Science and Engineering department as an Advisory Board member, a role that later expanded into being an Innovation Advisor within UCI's Beall Applied Innovation program. I also served on the Board of Directors at the Society of Clinical Research Associates, Inc. My career Maribelle Guloy
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