Oluwabunmi Akinwande

I’m a detail-oriented clinical research professional with over three years of experience supporting Phase I–IV clinical trials across cardiopulmonary and medical device studies. I focus on regulatory compliance, site management, data integrity, and monitoring support to help teams execute studies with confidence.

In my current role, I support the execution of four concurrent clinical trials by coordinating site initiation visits, monitoring visits, and audits while ensuring regulatory documentation is complete. I conduct patient pre-screening using EMR systems, obtain informed consent, enter and validate CRF data in EDC systems with ~98% data accuracy, and manage query resolution—cutting EDC backlog by 75% while improving data quality. I also process AE/SAE reporting on time, maintain ISF/TMF essential documents for audit readiness, and ensure investigational product accountability with no discrepancies.

I’m proud of results like increasing patient enrollment by 30% within six months, maintaining 100% audit readiness with no regulatory findings, and improving protocol compliance and visit adherence by 40% through process enhancements. Earlier clinical research support roles strengthened my patient-safety mindset through HIPAA-aligned documentation, protocol-required procedures, and clinical assessments—now I’m seeking to transition into an In-House CRA role to support monitoring, site oversight, and study execution.