• Associate Director , Oncology Clinical…

    Bristol Myers Squibb (Princeton, NJ)
    …with Biomarker Lead late stage clinical trials for Phases II/III preferred. Regulatory submissions drug approvals in solid tumor space also highly desirable. ... on translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to… more
    Bristol Myers Squibb (11/25/25)
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  • Director of AI Optimization…

    J&J Family of Companies (Titusville, NJ)
    …Johnson & Johnson Innovative Medicine (IM) is recruiting for a ** Director ** **of AI** **Optimization and** **Product** **ization** **- R&D Data Science ... is preferred. + Experience with Agile and DevOps methodologies + Experience with regulatory compliance and governance (eg GxP, SaMD, etc.). + Strong experience in… more
    J&J Family of Companies (11/19/25)
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  • Director , Program Management (PM)

    J&J Family of Companies (Titusville, NJ)
    …CAPLYTA(R) medical team to support our growing impact in psychiatry. The Director , Program Management (PM) is primarily responsible for leading the program ... Finance and Procurement, Global Commercial Strategic Organization, Global Medical Affairs, Regulatory Affairs, Research & Development, Global Safety, HR, HCC, Legal.… more
    J&J Family of Companies (10/30/25)
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  • Director , Technology Sales Support - NA…

    Wolters Kluwer (Trenton, NJ)
    …Consolidation & Reporting, CCH Tagetik has developed pre-packaged solutions addressing regulatory reporting requirements for ESG, Tax, Insurance & Banking. The ... **North American** team is seeking a ** Director of Solution Consulting, North America** to lead a...is pivotal in driving pre-sales excellence, aligning technical and business value, and supporting enterprise sales cycles across global… more
    Wolters Kluwer (10/09/25)
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  • Senior Director , AI Engineering,…

    Oracle (Trenton, NJ)
    …and modernize health systems globally. We are seeking a Senior Software Director to lead our AI engineering efforts across healthcare reimbursement, patient ... compliance** Ensure all AI solutions meet stringent security, privacy, and regulatory requirements (HIPAA and related standards). Partner with compliance and legal… more
    Oracle (11/25/25)
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  • Head of Global Product - Audit (Sr.…

    Grant Thornton (Iselin, NJ)
    …Key Responsibilities + Execute the global product strategy for Audit, aligning with business objectives and market needs. + Shape and communicate the product vision ... development and requirements gathering for Audit products, ensuring alignment with business needs and practitioner insights. + Build strong relationships with Audit… more
    Grant Thornton (10/30/25)
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  • Director Home Infusion

    Hackensack Meridian Health (Lodi, NJ)
    …day-to-day operations, which includes coordination of all activities, monitoring quality indicators, monitoring financial performance, and modeling a customer ... and long range plans and participates in strategic and business planning for the organization's home care services. Works...Manager of Clinical Practice to ensure that delivery of quality care is conforming to regulations, company standards, payor… more
    Hackensack Meridian Health (10/17/25)
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  • Director of Education, Governance…

    Bristol Myers Squibb (Princeton, NJ)
    …Read more: careers.bms.com/working-with-us . **Position Summary** At BMS, we believe business functions and Compliance & Ethics are equally accountable for both ... and payments. + Works to proactively manage risk factors including, changing regulatory requirements, reputational impact, and financial robustness. + A key point of… more
    Bristol Myers Squibb (11/07/25)
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  • Associate Director , Hypercell, Data…

    Bristol Myers Squibb (Summit, NJ)
    …across the cell therapy network.** **This role will work closely with Business Insights & Technology (BI&T) and cross-functional stakeholders to build robust data ... source systems.** + **Integrate structured and unstructured data from manufacturing, quality , and digital platforms into unified, accessible formats.** + **Support… more
    Bristol Myers Squibb (11/25/25)
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  • Associate Principal Scientist, Combination Product…

    Merck (Rahway, NJ)
    …with external partners. + Author and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs under ... in addition to device development expertise. + Strong familiarity with regulatory landscape associated with drug delivery combination product and design verification… more
    Merck (11/13/25)
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