• Quality Clinical

    RWJBarnabas Health (Oceanport, NJ)
    Quality Clinical and Regulatory Data Improvement CoordinatorReq #:0000221403 Category: Quality / Patient Safety Status:Full-Time Shift:Day ... is supporting department executive leadership in areas specific to clinical quality , patient safety events, regulatory...national benchmarking, NHSN, EPIC, Joint Commission resources and other clinical , payor or regulatory data more
    RWJBarnabas Health (12/11/25)
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  • Senior Principal Product Manager…

    Oracle (Trenton, NJ)
    …(HDI) is building the next generation of intelligent, cloud-based healthcare platforms - combining clinical , payer, and regulatory data at scale to transform ... you will lead the strategy, design, and delivery of regulatory and clinical data products...+ Ensure that our platform helps customers meet evolving regulatory , financial, and quality measurement requirements. This… more
    Oracle (11/25/25)
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  • Senior Specialist, Digital CMC Regulatory

    Merck (Rahway, NJ)
    …and relevant systems (LIMS, MES, SAP). + Experience in data governance, data stewardship, and data quality management in regulated environments. ... enabled by a dedicated application designed to create a frictionless flow of data from source systems to regulatory documentation. Under the guidance of… more
    Merck (12/02/25)
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  • Director of Clinical Data

    J&J Family of Companies (Raritan, NJ)
    …improvement. + In-depth understanding of clinical development, quality and regulatory standards and policies relevant to data management and data ... to drive increased efficiency, quality , performance, and innovation within the Clinical Data Acquisition functional area promoting the overall efficiency of… more
    J&J Family of Companies (12/10/25)
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  • Medical Device Regulatory Affairs…

    Oracle (Trenton, NJ)
    …decisions. Oracle also enables secure and compliant handling of sensitive healthcare data , helping organizations meet regulatory requirements and protect patient ... clinical protocols, design processes, and manufacturing procedures to maintain regulatory and quality compliance. + Maintain compliance with changing … more
    Oracle (11/25/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Trenton, NJ)
    clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes ... clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contribute… more
    Sumitomo Pharma (10/11/25)
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  • Lead Clinical Data Manager (Remote)

    IQVIA (Jersey City, NJ)
    …Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality , accuracy, and compliance while leading ... **IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across...promote best practices. + Drive process improvements and ensure regulatory and SOP compliance. **Who We're Looking For** Ideal… more
    IQVIA (10/31/25)
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  • Sr. Clinical Quality Specialist

    Terumo Medical Corporation (Somerset, NJ)
    …and applicable regulatory requirements, while driving continuous improvement in clinical quality systems and processes. Key responsibilities include planning ... Sr. Clinical Quality Specialist Date: Nov 19,...strategic input to clinical teams to ensure data integrity, regulatory compliance, and patient safety… more
    Terumo Medical Corporation (10/22/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …and strategic influence. Proven ability to lead teams in making timely, high- quality regulatory decisions that balance innovation, compliance, and enterprise ... while ensuring early integration of precision medicine approaches-including coordination of key regulatory and clinical documents to support drug and diagnostic… more
    Bristol Myers Squibb (12/03/25)
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  • Global Regulatory Affairs Device Lead…

    Sanofi Group (Morristown, NJ)
    regulatory authorities. You'll collaborate across R&D, Device, Manufacturing, and Quality teams while preparing high- quality regulatory submissions, ... relationships with Global Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality Groups within R&D and Manufacturing… more
    Sanofi Group (10/23/25)
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