Teams at Ocugen, Inc.

Supports Phase 1–3 clinical trials from site start-up through closeout. Coordinates investigational sites, CROs, vendors, and internal teams; monitors site performance, enrollment, data quality, safety follow-up, documentation, investigational product tracking, and regulatory readiness. Maintains CTMS, eTMF, study trackers, and metrics while supporting audits, inspections, budgets, invoices, and process improvements. Requires at least three years of clinical research experience and up to 20% travel.