• Audit Manager I- Treasury/Finance

    City National Bank (Jersey City, NJ)
    …audit methodology and taking into consideration industry development, emerging risks, and regulatory changes and expectations. WHAT WILL YOU DO? * Audit and ... Gathers and evaluates information received from business units and other external/ regulatory sources.Ability to multi-task and work in a dynamically changing… more
    City National Bank (08/07/25)
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  • Digital Biomarker Operational Lead

    Sanofi Group (Morristown, NJ)
    …teams, Digital Endpoint Strategy Leads, Project Leads, Study managers, Procurement, Regulatory , Quality, and others. . Lead and contribute detailed project ... analysis, and integration of digital data. . Share scientific, operational, and regulatory knowledge relevant to digital biomarkers. . Assist in building validation… more
    Sanofi Group (08/01/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more
    Merck (08/14/25)
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  • Sr. IT Principal Architect- Remote

    Prime Therapeutics (Trenton, NJ)
    …knowledge of data integration, data warehousing, streaming analytics, and data scientist solutions + Experience with the following technologies: Analytics and BI ... Pega Foundation for Healthcare, Salesforce Health Cloud) + Experience working with regulatory compliance requirements (HIPAA and/or PCI) + Previous experience in PBM… more
    Prime Therapeutics (08/14/25)
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  • Scientific Director, Drug Metabolism

    Bristol Myers Squibb (Princeton, NJ)
    …metabolic pathways to support drug discovery and development. More broadly, the scientist is expected to integrate this information with absorption, distribution and ... FIH, and strategies in 14C human ADME studies. + Understanding of regulatory requirements in the areas of drug metabolism, drug-drug interactions, bioanalysis,… more
    Bristol Myers Squibb (08/12/25)
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  • Director, R&D Data Science & Digital Health, RWE…

    J&J Family of Companies (Titusville, NJ)
    …team within Johnson and Johnson Innovative Medicines is looking for an outstanding scientist and leader who provides cross therapeutic area RWE expertise and whose ... trial data, observational databases, and literature reviews to support regulatory agency interactions. + Independently create study protocols, analysis plans,… more
    J&J Family of Companies (07/19/25)
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  • Product Manager, Predictive & Translational…

    Merck (Rahway, NJ)
    …roadblocks and engaging cross-functional experts to maintain progress. + Support regulatory audits and inspections by collaborating with stakeholders and Quality ... or chemistry. **Preferred Experience and Skills:** + Professional experience working as a scientist , Informatics Analyst or IT analyst in a drug discovery or… more
    Merck (08/19/25)
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  • Laboratory Solutions Lead

    CBRE (Trenton, NJ)
    …performance indicators. This position leads the overall relationship clients and scientist **What you'll do** Pricing Strategy Development: + Develop and implement ... + Reviews work to ensure compliance with performance, safety, statutory, and regulatory requirements, as well as with all company policies, standards, and… more
    CBRE (08/08/25)
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  • Med Tech/ Med Lab Tech Per Diem - Weekends/…

    Penn Medicine (Plainsboro, NJ)
    …all areas of testing performed .Adheres to all laboratory safety and regulatory practices .Communicates well with Physicians and other Ancillary services **What We ... OR REGISTRATION REQUIREMENT .Medical Technologist (ASCP or NCA), Medical Laboratory Scientist (ASCP), or previously qualified as Medical Technologist prior to… more
    Penn Medicine (08/07/25)
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  • Postdoctoral Researcher - Skin Biology

    Colgate-Palmolive (Piscataway, NJ)
    …a brighter, healthier future for all. Colgate-Palmolive is seeking a highly motivated scientist with a track record of excellence for a two year postdoc position ... to achieve project goals + Manage requirements involving legal agreements, IP, regulatory , safety and quality **Required Qualifications:** + Ph.D. in cell biology,… more
    Colgate-Palmolive (08/01/25)
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