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11 open roles read nightly from companies’ own hiring pages. Each one links to the original ad.

1–11 of 11 jobs

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  • Irvine Clinical Research · Los Angeles, California, United States +1

    On-siteFull-timeSenior$85K – $100K a yearScience & research

    Coordinate the day-to-day clinical operations of clinical research studies; Perform study procedures in accordance with GCP and study protocols; Organize and maintain paper and electronic study data in a complete and correct manner; Work closely with recruitment and…

  • Irvine Clinical Research · Arcadia, California, United States

    On-siteFull-time$80K – $90K a yearHealthcare

    Bilingual Clinical Prescreening & Screening: Conduct focused clinical interviews and medical history reviews in Mandarin and English to screen potential participants, efficiently identifying clear protocol exclusions while isolating viable candidates.; Participant & Family…

  • Irvine Clinical Research · Arcadia, California, United States

    On-siteFull-timeMid level$62.4K – $83.2K a yearScience & research

    Study Management: Serve as the primary or co-coordinator for assigned Phase II/III clinical research studies, overseeing day-to-day operations from site initiation to closeout.; Protocol Compliance: Execute study procedures with strict adherence to Good Clinical Practice (GCP)…

  • Irvine Clinical Research · Irvine, California, United States

    On-siteFull-time$80K – $90K a yearHealthcare

    Bilingual Clinical Prescreening & Screening: Conduct focused clinical interviews and medical history reviews in Mandarin and English to screen potential participants, efficiently identifying clear protocol exclusions while isolating viable candidates.; Participant & Family…

  • Irvine Clinical Research · Oakland, California, United States

    On-siteFull-time$80K – $90K a yearHealthcare

    Bilingual Clinical Prescreening & Screening: Conduct focused clinical interviews and medical history reviews in Mandarin and English to screen potential participants, efficiently identifying clear protocol exclusions while isolating viable candidates.; Participant & Family…

  • Irvine Clinical Research · Long Beach, California, United States

    On-siteFull-time$125K – $140K a yearHealthcare

    Clinical Trial Execution: Oversee and conduct protocol-driven clinical trial visits as a Sub-Investigator, ensuring strict adherence to FDA regulations, GCP guidelines, and study protocols.; Participant Eligibility & Medical Oversight: Conduct physical and neurological…

  • Irvine Clinical Research · Los Angeles, California, United States

    On-siteFull-time$125K – $140K a yearHealthcare

    Lead study team as a Sub-Investigator, ensuring trials are conducted safely and per protocol; Conduct clinical intake interviews to determine medical eligibility of potential study participants; Manage the safety of study participants; respond appropriately to adverse events in…

  • Irvine Clinical Research · Los Angeles, California, United States

    On-siteFull-timeMid level$62.4K – $83.2K a yearScience & research

    Study Management: Serve as the primary or co-coordinator for assigned Phase II/III clinical research studies, overseeing day-to-day operations from site initiation to closeout.; Protocol Compliance: Execute study procedures with strict adherence to Good Clinical Practice (GCP)…

  • Irvine Clinical Research · Riverside, California, United States

    On-siteFull-time$66.6K – $80K a yearScience & research

    Manage daily operations for assigned clinical trial projects; Perform study procedures in accordance with GCP and study protocols; Organize and maintain study data in a complete and correct manner in CRIO eSource/CTMS; Cultivate enthusiastic and professional relationships with…

  • Irvine Clinical Research · Riverside, California, United States +5

    On-siteFull-timeLead / staff$300K – $350K a yearHealthcare

    Lead study team as a Principal or Sub-Investigator, ensuring trials are conducted safely and per protocol; Conduct clinical intake interviews to determine medical eligibility of potential study participants; Educate potential participants about diseases and the benefits of…

  • Irvine Clinical Research · Irvine, California, United States +5

    On-siteFull-time$25.00 an hourPeople & HR

    Recruit study participants via short telephone interviews; make outbound phone calls to achieve appointment scheduling goal; Build rapport with potential participants to ensure engagement and retention; Promote Irvine Clinical Research's services and the opportunity to advance…

Updated 07 Nov 2026 10:21 UTC from the OptiTalent job library.