Worldwide Clinical Trials
Leticia Reyes, ASQ CQA, CPGP, CTBS, currently serves as Principal Scientist in Bioanalytical Study Management at Worldwide Clinical Trials, overseeing GLP and non-GLP clinical studies. Previously, Leticia held roles including QA Manager at Bone Bank Allografts, where compliance functions and Quality Control activities were led, and Validation Manager at GenCure, ensuring adherence to cGMP regulations. Additional experience includes roles at BPL Plasma as Compliance Manager and as Quality Manager at Azaya Therapeutics, managing Quality Systems and validating analytical methods. Leticia's career began at DPT Laboratories, culminating in a Senior Scientist position. Leticia holds a Master’s in Biotechnology and a Bachelor’s in Chemistry from The University of Texas at San Antonio.
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Worldwide Clinical Trials
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About Worldwide Clinical Trials Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.