Maria Gavides.

Clinical Research Operation Specialists

Founder,
Prime Trial Research Services

I help physician-led clinical research sites strengthen regulatory operations, improve screening performance, and build clear, efficient workflow systems.Venezuelan-trained physician with hands-on experience supporting Phase I–III clinical trials.Based in South Florida. Available for remote collaboration.

EXPERIENCE SNAPSHOT• 3+ years of clinical research experience• 5+ years of clinical medical experience• Phase I–III trial experience from site start-up through close-out• Specialized experience in pulmonology and dermatology research• Collaboration with investigators, sponsors, CROs, vendors, and site teams• Bilingual support in English and Spanish

Maria Gavides

Operational Focus

Clinical research sites manage multiple studies, patients, vendors, timelines, and regulatory requirements—often without a clear view of where operational gaps exist.I bring structure to those moving parts through organized start-up and regulatory workflows, screening and recruitment tracking, quality-control systems, and clear reporting—creating better visibility and more consistent study execution.

Maria Gavides

SITE SUPPORT SERVICES

• Regulatory document preparation and IRB submission coordination• Site start-up and study activation support• Essential document and ISF organization• Screening, recruitment, and enrollment tracking• Quality-control and documentation review• Workflow optimization, and remote site support