At Leidos Biomedical Research, I alert physicians to adverse events and protocol issues, coordinate regulatory filings, and assist with studies across the protocol lifecycle.
At the Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, NIH, I coordinated care and study procedures for patients with rare genetic disorders. I also recruited and enrolled trial participants, obtained informed consent, and quality-checked eCRFs.
At the Vaccine Research Center, National Institutes of Allergy and Infectious Diseases, NIH, I supported clinical trials involving investigational vaccines and related products. I monitored participant safety, documented adverse events, verified source records, and contributed to protocol and consent-form submissions.
Earlier, at University of Virginia Transitional Care Hospital (UVA), I provided care for complex cases and coordinated clinical responses. My work has included Phase I–III research, GCP, informed consent, and regulatory compliance.
