Jobs 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.

Coordinate day-to-day clinical trial operations, perform study procedures per protocol and GCP, manage paper and electronic study data, recruit and screen participants, and conduct diagnostic, efficacy, and safety assessments.

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 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 Coordinator I will manage day-to-day operations of clinical trials, including participant recruitment and data management under supervision.

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

The Clinical Scientist/Neuropsychological Rater will assess study participants, conduct interviews, inform about clinical trials, and assist with study operations.

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.