• Senior GCP Compliance

    AbbVie (North Chicago, IL)
    …procedures in place to support the clinical trial conduct and their overall compliance with ICH GCP guidelines, applicable regulations, and the organization's ... guidelines, policies and procedures. + Plan, organize and lead multiple GCP vendor compliance audits on a global scale. + Initiate, manage, and participate… more
    AbbVie (04/01/24)
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  • Good Clinical Practice ( GCP

    GE HealthCare (Boston, MA)
    **Job Description Summary** The Good Clinical Practice ( GCP ) Senior Quality Assurance (QA) Auditor is crucial in ensuring that clinical trials are conducted ... ethically, with integrity, and in compliance with regulatory requirements and GCP guidelines. This role is responsible for providing QA auditing for the PDx… more
    GE HealthCare (02/23/24)
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  • Senior Good Clinical Practice ( GCP

    Philips (Orange, OH)
    The Senior Good Clinical Practice ( GCP ) Auditor will play a critical role in ensuring Philips' Clinical Studies and practices are compliant with ... + Planning, coordinating, and executing clinical audits to assess clinical study compliance with Good Clinical Practice ( GCP ), regulatory standards, and study… more
    Philips (04/13/24)
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  • Quality Assurance Auditor 2 - Hybrid

    IQVIA (Durham, NC)
    We are seeking a **Quality Assurance Auditor 2** to join Q2 Solutions, IQVIA's laboratory business in Durham, NC. We hire passionate innovators who drive healthcare ... as we transform and accelerate research and development. As a Quality Assurance Auditor 2, you will plan, conduct, and report assigned quality assurance audits,… more
    IQVIA (04/26/24)
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  • Clinical Research Monitoring Specialist…

    University of Pennsylvania (Philadelphia, PA)
    …as well as assisting with corrective actions and training related to research compliance , quality control and quality assurance. The monitor/ auditor will follow ... resources, and much more. Posted Job Title Clinical Research Monitoring Specialist Senior (Cancer Center) Job Profile Title Clinical Research Monitoring Specialist … more
    University of Pennsylvania (04/25/24)
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  • Clinical Research Specialist-CCTO

    Weill Cornell Medical College (New York, NY)
    …clinical research studies. **Job Responsibilities** + Coordinate clinical trials in compliance with federal regulations, GCP guidelines, and internal policies. ... to facilitate the screening, enrollment, and treatment of research subjects in compliance with established regulations and guidelines and internal SOPs. + Assists… more
    Weill Cornell Medical College (04/19/24)
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  • Sr Health Project Coord

    University of Rochester (Rochester, NY)
    …and non-departmental personnel to assure that this institution is in compliance with study guidelines as detailed on the individual treatment protocols. ... Ensure timely submission of this study data. Regulatory + Ensures compliance with acceptable regulatory requirements and IRB standards. The regulatory agencies… more
    University of Rochester (03/31/24)
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  • Quality Ops Manager

    PCI Pharma Services (Philadelphia, PA)
    …Operations Manager Department/Group: QC Inspection Location: Philadelphia Reports to: Senior Quality Operations Manager FLSA Status: Exempt Summary of Objective: ... overseeing the direction, training, organization, alignment, monitoring, and cGMP compliance to ensure we deliver a safe and quality...quality product. This position will oversee both the Quality Auditor and Label Room teams. This is a supervisory… more
    PCI Pharma Services (02/13/24)
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