Clinical Research Associate with nearly five years of experience supporting end-to-end clinical trial operations. Experienced in interpreting clinical protocols, translating Schedule of Events into operational workflows, training investigators and site staff, conducting site activation activities, and supporting implementation of clinical technology platforms. Proficient with multiple EDC, IRT, eCOA, and CTMS systems, with hands-on User Acceptance Testing (UAT) experience and a strong commitment to ICH-GCP, quality, and continuous process improvement.