• Data Scientist II (US)

    TD Bank (Mount Laurel, NJ)
    …II who will perform the quantitative analysis, model development, model review and related research to meet the business requirements of the team. This is a critical ... or ongoing use + Compile and generate ad-hoc analytical reports + Lead research efforts, applying expertise in statistical analysis and modeling + Provide advisory… more
    TD Bank (08/23/25)
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  • Senior Specialist, Scientific Reference Data

    Merck (Rahway, NJ)
    **Job Description** Be part of a dynamic team that is dedicated to accelerating research and innovation. We are seeking a passionate Senior Specialist to join our ... a background in pharma/biotech. Previous experience with implementing and managing clinical and regulatory data standards is a big plus. If you believe in the power… more
    Merck (08/22/25)
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  • Associate Director, Competitive Intelligence

    Sumitomo Pharma (Trenton, NJ)
    …diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more ... cross-functional stakeholders, including in Commercial, Clinical Development, Medical Affairs, Regulatory , Sales leadership and Finance/IR functions. **Job Duties and… more
    Sumitomo Pharma (08/20/25)
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  • Digital Biomarker Operational Lead - VIE Contract

    Sanofi Group (Morristown, NJ)
    …with Study Teams, Project Managers, Digital Endpoint Strategy Leads, Procurement, and Regulatory to align on study-specific needs. + Attend and document project ... (including studies) in a combination of biomedical engineering, clinical research , digital biomarker operations, clinical operations, study management, or medical… more
    Sanofi Group (08/13/25)
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  • Asst Director Patient Care , Pre/Post Surgical

    RWJBarnabas Health (New Brunswick, NJ)
    …priorities for patient care needs. Serving as a resource for interpretation of regulatory requirements . Assumes key functions in implementation of P&P of nursing ... based knowledge and skills both formally and informally + Incorporating current research findings into clinical practice Provides open lines of communication for… more
    RWJBarnabas Health (08/01/25)
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  • (Senior) Data Team Lead

    IQVIA (Jersey City, NJ)
    …Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. ... do not align with an Analyst, Architect Data Entry, Design, Engineering, IT, or Research role. Applicants that do not meet the requirements for the position will not… more
    IQVIA (08/01/25)
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  • Senior Manager, Statistics (office based)

    AbbVie (Florham Park, NJ)
    …and innovations in drug development spanning trial design, monitoring and regulatory submissions, as well as post-marketing access. As a Senior Manager, ... Statistics you will provide statistical leadership to support the research and development organization for assigned projects. Specific areas of work may include… more
    AbbVie (07/29/25)
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  • R&D Assistant- Household, US (Essential Home)

    Reckitt (Montvale, NJ)
    …highest quality hygiene, wellness, and nourishment a right and not a privilege. **​ Research & Development​** In Research and Development, we're full of highly ... skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine… more
    Reckitt (07/12/25)
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  • Account Director, Platform Success - IQVIA Digital…

    IQVIA (Parsippany, NJ)
    …global provider of data, advanced analytics, technology solutions and clinical research services for the life sciences industry. Learn more at www.iqviadigital.com ... a trusted industry expert, providing clients with guidance on market shifts, regulatory changes, and evolving best practices. Represent the company in high-profile… more
    IQVIA (07/04/25)
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  • Clinical Coordinator (RN) Cancer Center (Days)

    RWJBarnabas Health (Livingston, NJ)
    …transplantation and IEC therapies while ensuring informed consent documentation + Support Research & Clinical Trials - Assist with enrolling patients in clinical ... trials, comply with regulatory reporting requirements (FACT,... reporting requirements (FACT, CIBMTR, NMDP, IRB), and facilitate research data collection + Maintain Communication & Documentation -… more
    RWJBarnabas Health (06/30/25)
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