Teams at Irvine Clinical Research

Coordinate Phase II/III clinical trials onsite: manage study operations, ensure GCP/FDA protocol compliance, enroll and coordinate participants, perform clinical assessments (vitals, ECGs), enter and maintain eSource/EDC/CTMS data, and maintain regulatory readiness for monitoring and audits.

Provide clinical oversight as a Sub-Investigator for Alzheimer’s disease trials: screen participants, manage safety and adverse events, perform exams, infusions, phlebotomy, and coordinate with physicians and study coordinators to ensure protocol compliance and participant care.

The clinician will oversee clinical trials for Alzheimer's Disease treatments, manage safety, conduct eligibility interviews, and perform assessments.