• Senior Solution Consultant

    Norstella (Trenton, NJ)
    …services and Real World Data (RWD) offerings to support use cases across the clinical lifecycle including clinical trial planning, feasibility, and patient ... support activities **Qualifications:** * 5+ years experience in working in clinical trial relevant business either CRO, trial recruitment, consulting, or… more
    Norstella (08/08/25)
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  • Sr. Scientist, Statistical Programming- PKPD…

    Merck (Rahway, NJ)
    …Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** + Effective interpersonal… more
    Merck (08/26/25)
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  • Principal Field Clinical Engineer- North…

    Medtronic (Newark, NJ)
    …regulatory compliance guidelines for clinical trials. + Experience in clinical studies and/or trial site management/protocols. + Experience collaborating ... ​ Travel up to 70%. In this exciting role as the **Principal Field Clinical Engineer (FCE)** for the Cardiac Ablation Solutions Operating Unit, you will be… more
    Medtronic (08/22/25)
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  • Associate Director, Quantitative Pharmacology…

    Merck (Rahway, NJ)
    …+ Develop model-based strategies (translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within ... phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. + Represent QP2 on cardiometabolic and… more
    Merck (08/21/25)
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  • Head of Execution, Planning, Innovation…

    Teva Pharmaceuticals (Parsippany, NJ)
    …in harmonizing processes across Innovative and Generics and ensuring seamless execution of clinical trial operations worldwide. The EPIX group will act as the ... improvement to enable high-quality, timely, cost effective, and patient centric clinical trial delivery **Key Responsibilities:** + Provide visionary leadership… more
    Teva Pharmaceuticals (08/20/25)
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  • Principal Scientist, Biostatistics

    Merck (Rahway, NJ)
    …data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials. The knowledge ... analyzing clinical trials and coordinating the statistical activities for clinical trial projects; and may lead a group of statistical or programming staff… more
    Merck (07/16/25)
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  • Senior Director, Quantitative Science - Princeton,…

    dsm-firmenich (Princeton, NJ)
    …analytics and modeling- from early target identification and disease modeling to clinical trial analytics, product claims support. Sound intriguing? There's ... high-throughput screening data; guide development of computational disease models; lead clinical trial data foundation, analytics, and interpretation, ensuring… more
    dsm-firmenich (08/26/25)
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  • Research Financial Analyst II

    Hackensack Meridian Health (Edison, NJ)
    …for providing support in the preparation of all financial aspects of grant and clinical trial reporting which include, preparation of budgets for grant / ... clinical trial applications, general ledger grant/ clinical trial revenue and expense analysis, submission of monthly, quarterly, and/or annual grant/… more
    Hackensack Meridian Health (07/02/25)
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  • Oncology Regional Medical Scientific Associate…

    Merck (Trenton, NJ)
    …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... License:** Yes **Hazardous Material(s):** n/a **Required Skills:** Advisory Board Development, Clinical Engagement, Clinical Trial Support, Gastrointestinal… more
    Merck (08/23/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Trenton, NJ)
    …experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's Degree in ... in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years of experience in vendor… more
    United Therapeutics (08/21/25)
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