Sandra McGriff is a Clinical Research Associate I at Fortrea, responsible for site monitoring and management in clinical trials. With extensive experience in clinical operations, Sandra has previously served as a Clinical Trial Manager at Twill, overseeing trials for a decentralized digital therapeutic device sponsor. Prior roles include Research Project Manager at Cherokee Nation Businesses, where Sandra managed pre-clinical and clinical research studies, and Clinical Research Regulatory Specialist at STAR Clinical Trials, where regulatory compliance was prioritized. Sandra's career began as a Clinical Research Assistant at CEDRA Clinical Research and progressed through various positions, including Clinical Research Manager and Clinical Research Coordinator. Sandra holds a Master's degree in Health Services Research from Texas State University and a Bachelor of Science in Biology from The University of Texas at San Antonio.
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