➤Clinical trial data management and data integrity specialist with 13 years of experience supporting regulated research and industry‑sponsored oncology imaging trials across academic and clinical environments.
➤I help early‑stage biotech, sponsors, and CRO teams ensure accurate, inspection‑ready clinical trial data through hands‑on support in clinical data mining, EMR–EDC traceability, source‑to‑CRF reconciliation, query review and resolution, and cross‑system data alignment.
➤My work focuses on translating protocols into practical data workflows, identifying data inconsistencies early, and strengthening data integrity across sites, vendors, and clinical systems.
➤I am best suited for projects that require structured data review, strong documentation standards, and close collaboration between clinical operations, data management, and regulatory stakeholders.