Bukola Amos

I am a Senior Clinical Research Associate with over nine years of experience leading Phase I–IV global clinical trials across oncology, neurology, infectious disease, ophthalmology, cardiovascular disease, and medical devices. I bring a disciplined, detail-driven approach to remote and on-site monitoring, data integrity, and cross-functional collaboration.

I have managed large site portfolios (40–60+ sites), implemented risk-based monitoring strategies that reduced protocol deviations by ~30%, and maintained ~99% data accuracy to support on-time database locks. I ensure inspection readiness through meticulous eTMF and regulatory documentation maintenance, contributing to zero major audit findings across multiple studies.

I mentor junior CRAs, standardize monitoring practices, and coordinate effectively with sponsors, CROs, investigators, and internal teams to resolve issues proactively, improve site performance, and safeguard patient safety—delivering measurable improvements in study timelines and data quality.