Latrise Holt

I am a detail-oriented clinical trials professional with over two years of experience supporting CRO and sponsor-dedicated trials, grounded in a science-based bachelor's degree and a clear understanding of drug development, FDA regulations, and ICH GCP.

As a Clinical Trials Associate I maintained the Trial Master File, assisted with IRB submissions and ICF language updates, coordinated system access and training, and managed CTMS/EDC documentation to ensure timely task completion and regulatory compliance.

My background in pharmacy and laboratory roles strengthens my focus on patient safety, specimen integrity, and operational accuracy; I seek opportunities to contribute to study start-up, vendor management, and clinical operations while continuing to grow my regulatory and project coordination expertise.