• Manager, Global Quality Management - Clinical…

    Otsuka America Pharmaceutical Inc. (Springfield, IL)
    …: Plan, conduct, and report GCP audits of CROs, clinical laboratories, and investigator sites globally, ensuring compliance with ICH-GCP, local regulations, and ... : Maintain audit metrics and contribute to management reporting on audit outcomes, trends, and compliance risks. **Qualifications** Required + Bachelor's… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Sr. Clinical Research Associate - Oncology - FSP

    Parexel (Springfield, IL)
    …the quality of investigator sites (eg patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and ... the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance… more
    Parexel (12/11/25)
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  • Senior Clinical Research Associate/Clinical…

    Parexel (Springfield, IL)
    …the quality of investigator sites (eg patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and ... the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance… more
    Parexel (12/07/25)
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  • Clinical Research Coordinator I - Neurology…

    Rush University Medical Center (Chicago, IL)
    …0.9 and 1.0) **Shift:** Shift 1 **Work Schedule:** 8 Hr (7:00:00 AM - 3 :00:00 PM) Rush offers exceptional rewards and benefits learn more at our Rush benefits ... studies across a range of disciplines. Receives direction from principal investigator , supervisor, or other staff involved in research protocol(s). Responsibilities… more
    Rush University Medical Center (12/20/25)
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