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Senior Clinical Research Associate
Senior Clinical Research Associate at Biolife genetics, reducing clinical data query resolution by 35% across Phase I–IV trials.
United StatesSenior Clinical Research Associate at Biolife Genetics
Conducted independent site qualification, initiation, interim monitoring, and closeout visits for Phase I–IV cardiovascular, metabolic, and oncology studies. Improved clinical data query resolution by 35% and reduced protocol deviations by 30% through risk-based monitoring and CAPA implementation.
CTMSEDCICH GCPFDA RegulationsSource Documentation Verification (SDV)Risk Based MonitoringCAPAPatient SafetyClinical Trial MonitoringSite management
Performed on-site and remote monitoring visits for multicenter clinical trials, reviewing source documents and electronic case report forms. Improved monitoring report turnaround time by 35% and reduced unresolved site findings by 30%.
CTMSETMFEDCICH GCPDocument ReviewProtocol Deviation TrackingSite InitiationInvestigator TrainingClinical Trial Agreements
Prepared and handled biological samples using calibrated micropipettes, centrifuges, and Biological Safety Cabinets. Improved sample tracking accuracy by 35% and reduced manual inventory processing time by 30%.
LIMSExcelSample Trackinglaboratory operationsAseptic TechniqueBiological Safety CabinetsInventory ManagementSOPs
Master of Health Administration degree from Walden University.
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