
Experienced clinical research professional with hands-on involvement in over 80 oncology trials, supporting regulatory documentation, system updates, and study maintenance across CTSU, NCI CIRB, and DDOTS. Strong background in reviewing protocols, maintaining accurate records, and ensuring compliance with GCP and IRB requirements. Known for improving documentation processes, creating clear execution guidelines, and supporting CRAs and study teams by keeping systems organized, accurate, and audit-ready throughout the trial lifecycle.