
Detail‑oriented Clinical Research Coordinator with 5+ years of experience supporting oncology and multi‑site clinical trials. Skilled in regulatory compliance, data management, and patient engagement, with a proven record of improving trial efficiency and maintaining meticulous documentation. Adept at managing electronic data capture (EDC) systems, EMRs, and MS Office tools to ensure accuracy and audit readiness. Recognized for safeguarding patient confidentiality, fostering cross‑functional collaboration, and driving process improvements that enhance study operations. Creative problem‑solver with strong organizational, time management, and project leadership abilities.
Technical Skills
Core Competencies