Jobs 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.

Conduct Mandarin- and English-language prescreening, clinical interviews, medical history reviews, cognitive and psychiatric rating scales, and participant enrollment for Phase II/III neurology and psychiatry trials. Engage participants and families, build evidence-based eligibility cases, administer standardized assessments, collaborate with investigators and research teams, support documentation and trial operations, and conduct community outreach among Mandarin-speaking populations.

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.

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.

Provide front-desk administrative support for a clinical research center: greet and assist (especially older adults), coordinate and troubleshoot participant scheduling, learn protocols and enter data, assist clinicians during visits, and perform clerical tasks while committing to at least two years of growth.

The Clinical Research Coordinator manages clinical trial operations, ensures compliance with protocols, and works on patient recruitment and assessment, with a focus on Alzheimer's research.

The Research Assistant will provide administrative support to physicians and researchers, assist with data entry, manage scheduling, and greet participants, particularly older adults.

The Clinical Research Recruitment Coordinator recruits study participants through phone interviews, promotes services, and manages data input and outreach efforts.

The Neurologist Principal Investigator will lead clinical trials in memory disorders, manage trial safety, educate participants, and oversee a study team.

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.

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.