Teams at Irvine Clinical Research

Manage daily operations of clinical trials, perform study procedures per GCP and protocols, maintain paper and electronic study data, engage patients and sponsors, work with recruitment to meet enrollment goals, and conduct diagnostic, efficacy, and safety assessments.

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 Research Nurse will administer investigational drugs, monitor participant safety, perform medical procedures, and ensure accurate study data collection.