Erin Snodgrass

I lead and coordinate Phase II–IV clinical trial activity across multiple therapeutic settings, with a focus on compliance with research protocols, regulatory requirements, quality standards, and sponsor expectations. I bring an operations-first mindset that keeps studies moving while maintaining rigor.

Previously, I coordinated Phase II and Phase III pharmaceutical, NCI-sponsored, and investigator-initiated trials from study start-up through final close-out. I supported the full lifecycle with an emphasis on documentation accuracy and readiness for each protocol milestone.

I’ve also supported clinical trial execution through subject eligibility review, documentation management, data entry, event reporting, and research committee coordination. I’m comfortable handling high-detail workflows where timely updates and clean records directly impact study continuity.

Across my experience, I prioritize consistent execution, careful attention to quality, and clear coordination with internal teams and trial stakeholders. I’m energized by roles where I can strengthen trial operations and regulatory compliance to help deliver reliable, sponsor-aligned results.