At Ardent Health Services, I manage six active clinical trial sites and conduct on-site and remote monitoring visits for Phase II/III metabolic and CNS studies. I reduced protocol deviations by 35% through targeted site retraining, root cause analysis, CAPA support, and follow-up.
I also improved eCRF data accuracy by 15% across assigned sites and achieved 98% query resolution within five business days. My monitoring work includes source data review and verification, safety and investigational product review, and monitoring documentation.
Previously at PolyCRA, I conducted monitoring for oncology, gastroenterology, and endocrinology studies as a Clinical Research Associate I, after coordinating rheumatology study activities there. I’m an ACRP-certified Clinical Research Associate and hold a Project Management Professional certification.
