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.

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.

Coordinate Phase II and III clinical trials from site initiation through closeout, ensuring protocol compliance, patient safety, data integrity, and audit readiness. Manage participant consent, screening, visit schedules, clinical assessments, and cross-functional appointments. Maintain regulatory and source documentation, enter data in eSource, EDC, and CTMS platforms, resolve queries, and support sponsor monitoring and audits.