Teams at Texas Diabetes & Endocrinology, P.A.

Supports Phase II–IV clinical trials under Principal Investigator supervision. Responsibilities include participant screening, recruitment, consent, clinical procedures, specimen handling, investigational product management, adverse event reporting, source documentation, data collection, regulatory compliance, and audit readiness. The coordinator communicates with participants, sponsors, laboratories, CRAs, and internal research staff while maintaining protocol, GCP, IRB, and safety requirements.