Teams at Irvine Clinical Research

Conduct bilingual Mandarin-English prescreening, clinical interviews, medical history reviews, cognitive and psychiatric rating scales, and participant enrollment for Phase II/III outpatient trials. Engage participants and families, explain trial requirements and safety, synthesize diagnostic evidence, advocate for eligible candidates, collaborate with investigators and sponsors, and support documentation, community outreach, and site operations. Experience with older adults, MCI, Alzheimer’s disease, or clinical trial rating is preferred.

Supports clinical trial operations through bilingual participant communication, reception, scheduling, visit coordination, vital signs, ECGs, screening, specimen processing, translation, EDC data entry, documentation, inventory tracking, and query resolution. The role requires compassionate service for elderly and vulnerable participants, strict protocol adherence, and full-time on-site availability.

Conducts protocol-driven Alzheimer’s disease clinical trial visits as a Sub-Investigator. Responsibilities include participant eligibility assessments, physical and neurological examinations, medical history reviews, IV placement, investigational medication infusions, safety monitoring, adverse-event reporting, and collaboration with Principal Investigators and research staff. The role requires an active California NP or PA-C license, infusion proficiency, experience with older adults, strong documentation, and compassionate communication. Prior pharmaceutical trial research experience is preferred but not required.