Teams at Irvine Clinical Research

Conduct bilingual Mandarin-English prescreening and screening interviews for Phase II/III neurology and psychiatry trials. Review medical histories, assess protocol eligibility, administer and score cognitive and psychiatric scales, engage participants and families, build evidence-based eligibility cases, collaborate with investigators and sponsors, and support enrollment, outreach, documentation, and trial operations.

Coordinate Phase II and III clinical trials from site initiation through closeout. Manage participant consent, screening, visits, assessments, and cross-functional appointments while ensuring GCP, FDA, and protocol compliance. Maintain accurate data in eSource, EDC, and CTMS systems, resolve queries, preserve regulatory documentation, and support sponsor monitoring visits and audits. Conduct vital signs, ECGs, and other protocol-specific assessments while partnering with investigators and clinical staff.

Supports clinical trial operations by conducting bilingual participant prescreening, assisting with study visits and clinical procedures, translating communications and consent materials, maintaining source documentation, entering data into EDC systems, scheduling participants, and supporting Mandarin-language community outreach.