• Clinical Research Coordinator

    Hackensack Meridian Health (Neptune City, NJ)
    …in science or healthcare field. + Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years ... to transform healthcare and serve as a leader of positive change. The ** Clinical Research Coordinator** is responsible for coordinating and overseeing clinical more
    Hackensack Meridian Health (08/24/25)
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  • Principal Field Clinical Engineer- North…

    Medtronic (Newark, NJ)
    …lab, biomedical engineering, hospital/clinic or medical sales. + Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for ... ​ 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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  • Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …+ 10+ Years with MS/MA or MBA **PREFERRED QUALIFICATIONs:** + Proficiency in clinical regulatory requirements (Global) is a must. + Expert-level experience ... improvements in R&D quality processes, systems, and standards to meet regulatory requirements and organizational goals and contribute to the overall quality… more
    Gilead Sciences, Inc. (08/21/25)
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  • Clinical Coordinator (RN) Cancer Center…

    RWJBarnabas Health (Livingston, NJ)
    …Research & Clinical Trials - Assist with enrolling patients in clinical trials, comply with regulatory reporting requirements (FACT, CIBMTR, NMDP, IRB), ... Clinical Coordinator (RN) Cancer Center (Days)Req #:0000204916 Category:Nursing...quality meetings to support ongoing program improvements + Ensure Regulatory Compliance - Stay updated on policies and procedures… more
    RWJBarnabas Health (06/30/25)
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  • Principal Scientist, Biostatistics

    Merck (Rahway, NJ)
    …design, computing software and data management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase ... sound scientific principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions. This… more
    Merck (07/16/25)
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  • Director, Statistics (Office-based)

    AbbVie (Florham Park, NJ)
    …projects. A visible and collaborative role, the Diector works in partnership with clinical and regulatory experts to advance medicines to our patients. ... development and drive alignment with functional management. Partner with other functions ( Clinical , Regulatory , Patient Safety, or GMA) to create development… more
    AbbVie (08/23/25)
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  • Scientific Director/Senior Scientific Director,…

    Bristol Myers Squibb (New Brunswick, NJ)
    …Project Team objectives and encompass drug substance, drug product, analytical, quality, regulatory , and clinical supplies. + Represents the Global Product ... on key R&D Project Teams, actively collaborates across functional areas ( Clinical , Commercial, Regulatory , Clinical Pharmacology, Toxicology, etc.)… more
    Bristol Myers Squibb (08/26/25)
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  • Associate Director, Statistics - Immunology

    AbbVie (Florham Park, NJ)
    …development and drive alignment with functional management. Partner with other functions ( Clinical , Regulatory , Patient Safety, and GMA, etc.) to create ... Associate Director, Statistics - Immunology provides statistical leadership for clinical development and life-cycle management strategies for assigned projects.… more
    AbbVie (07/16/25)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Jersey City, NJ)
    …project timelines. **Preferred Experience and Skills** A candidate with experience in Regulatory CMC in clinical development, initial marketing application and ... Scientist (Associate Director) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small… more
    Organon & Co. (07/22/25)
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  • Global Project Head, Rare

    Sanofi Group (Morristown, NJ)
    …dotted-line management toward all GPT members, including eg project management, clinical operations, regulatory , safety, translational medicine, statistics, CMC, ... The GPH will be delegated such responsibilities as interaction with regulatory /health authorities (HA), approval of documents and product label, as appropriate.… more
    Sanofi Group (07/30/25)
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