I'm a clinical research professional with over 5 years of successfully supporting sponsor, CROs, and research sites in executing protocol-compliant and audit-ready clinical trials across EU, APAC, and US.
I’ve led and monitored Phase I–IV clinical trials from start-up through close-out, contributing to streamlined site activations, timely regulatory approvals, and ensuring data quality aligned with regulatory and ICH-GCP standards. My contributions have helped deliver trials that are ethical, compliant, and meaningful for both patients and the scientific community.
Whether you're setting up a new study or looking to improve site operations, I’m here to support your goal. Let’s connect and work together to deliver clinical trials that are compliant, ethical, and truly impactful.
