Senior Clinical Research Associate with 9+ years of progressive experience across CROs, biotech, and sponsor environments. Proven expertise in end-to-end clinical trial monitoring, sponsor oversight, and site management across Phase I–IV studies. Strong background in oncology and medical devices, with demonstrated ability to ensure GCP/ICH compliance, drive data quality, and support cross-functional clinical operations. Recognized for leadership in CRA mentoring, audit readiness, and risk-based monitoring.