Cecillia Diaz, LVN, CCRC, is an experienced clinical research professional with a diverse background in leadership and quality assurance. As Site Director at ObjectiveHealth, Cecillia oversees operational functions, while previous roles include QA Consultant at Sarah Cannon Research Institute and Clinical Study Manager for Early Phase Services at Worldwide Clinical Trials. Additionally, Cecillia served as Executive Director of Clinical Research Operations at Impact Research Institute and was the Austin Site Manager and Quality Control Associate at Pinnacle Clinical Research.
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