ObjectiveHealth
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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ObjectiveHealth
ObjectiveHealth is a leading integrated research provider partnering with physicians and healthcare organizations to establish advanced infrastructure for research programs. The company takes an innovative approach to research that aims to improve patient outcomes at the point-of-care. Utilizing proprietary technology, processes and trained on-site personnel, ObjectiveHealth delivers significant advances in the conduct of clinical research, benefiting clients and partners while providing broader care options for patients. Approaching 31 partnered programs across 16 states and over 600 providers, ObjectiveHealth is poised for continued growth due to the realized value of their healthcare solutions for all stakeholders.