• Staff Ethics and Investigations Partner

    Intuit (San Diego, CA)
    …will report to the Director, Ethics & Investigations. **What you'll do:** As an investigator , you will work as part of a dynamic team responsible for investigating ... harassment, retaliation, workplace bullying, and reported financial, expense, and compliance matters. You will manage a caseload of multiple investigations,… more
    Intuit (07/17/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …an assigned set of multiple research protocols assuring efficiency and regulatory compliance . These studies will be conducted at the Stanford Hospital and Clinics. ... Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of… more
    Stanford University (08/07/25)
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  • Research Administrator

    University of Southern California (Los Angeles, CA)
    …Manage financial aspects of clinical trials, including budget tracking, investigator payments, invoices, and financial reporting for sponsors. + Proposal ... & Financial Oversight: Develop, prepare, and monitor project budgets, ensuring compliance with financial and institutional policies. + Regulatory Compliance :… more
    University of Southern California (06/27/25)
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  • Research Coordinator I

    University of Southern California (Los Angeles, CA)
    …and feasibility of required study tests, at areas pertaining to patient compliance , dose modification and at drug toxicities. At times will provide information ... based on toxicity may be necessary and require recalculation. 2. Protocol Compliance a. Ensures correct date for return clinic appointment or hospital admission.… more
    University of Southern California (08/08/25)
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  • Clinical Research Coordinator 2 (6 Month…

    Stanford University (Stanford, CA)
    …work. + Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing ... define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study… more
    Stanford University (08/07/25)
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  • SOC Team Lead - FedRAMP

    Rubrik (Palo Alto, CA)
    …environment. **What you'll do:** + Lead and act as the primary investigator during incident response (IR) activities, leveraging expertise in enterprise forensics. ... NIST, SANS). + Demonstrable experience working in environments subject to FedRAMP compliance (eg, experience with NIST SP 800-53, FedRAMP controls, JAB/Agency ATO… more
    Rubrik (08/07/25)
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  • Clinical Research Coordinator 2 - GI & Hepatology…

    Stanford University (Stanford, CA)
    compliance . Regularly inspect study document to ensure ongoing regulatory compliance . + Work with principal investigator to ensure Investigational New ... work. + Audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing… more
    Stanford University (08/07/25)
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  • Cancer Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …and clinical staff to support clinical trial conduct, maintaining regulatory compliance , and providing general communication with both internal and external ... study related documents, and complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case report forms for… more
    Stanford University (08/07/25)
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  • SCI Senior Regulatory Specialist (Hybrid)

    Stanford University (Stanford, CA)
    …team of regulatory experts responsible for the administration and regulatory compliance of clinical research within the university, and represent the university ... attention to detail. We strive for top-quality regulatory support of investigator -initiated clinical trials with a high degree of professionalism, initiative and… more
    Stanford University (08/07/25)
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  • Clinical Research Associate

    University of Southern California (San Diego, CA)
    …remote monitoring for assigned clinical sites and co-monitor visits. Review Investigator Site Files, study data, perform IP reconciliation, review Informed Consent ... study participants. Conduct monitor review of eCRFs. Ensure participant safety and protocol compliance . + Act as main point of contact for assigned clinical sites. +… more
    University of Southern California (06/11/25)
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