• Associate Director, US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …growth, thereby accomplishing corporate goals. **Responsibilities** + Develop and implement US regulatory strategy for assigned project (s). + Strategize and plan ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Summary** This role… more
    Daiichi Sankyo Inc. (06/19/24)
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  • Associate Director, External Sponsored…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …both strategy formulation and operational execution in the field of externally sponsored research . Provide clear direction and guidance to project teams. + ... primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. **Summary:** The … more
    Daiichi Sankyo Inc. (07/27/24)
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  • Clinical Research Associate I Safety…

    The Mount Sinai Health System (New York, NY)
    …safety findings in a summary format to the Associate Director of Research and Quality Outcomes. + Interfaces with project management, functional team members ... **JOB DESCRIPTION** The Clinical Research Associate is an integral part...clinical study reports of assigned projects for submission to regulatory authorities. **QUALIFICATIONS** Education: + Bachelors Degree in life… more
    The Mount Sinai Health System (08/02/24)
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  • Associate Director, IT Research

    Merck (Rahway, NJ)
    **Job Description** ** Associate Director, IT Research Automation Engineer in RaDS** **IT** RaDS IT Research Infrastructure Product Line (RIPL) engineering ... team is seeking an Associate Director - Research Laboratory Automation Engineer....scientists and engineers to identify automation needs and define project requirements. + Collaborate with instrument vendors and suppliers… more
    Merck (09/04/24)
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  • Regulatory Compliance Risk Senior…

    Grant Thornton LLP (New York, NY)
    As a Banking Compliance Risk Senior Associate , you will get the opportunity to grow and contribute to our banking clients' business needs by providing in-depth ... on emerging regulations and help organizations leverage efficiencies within the Regulatory Compliance Practice - all with the resources, environment, and support… more
    Grant Thornton LLP (09/14/24)
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  • Regulatory Compliance Risk Senior…

    Grant Thornton LLP (New York, NY)
    As a Regulatory Compliance and Operational Risk Senior Associate , you will get the opportunity to grow and contribute to our clients' business needs by providing ... to provide comprehensive compliance optimization strategies, to help clients remediate regulatory gaps, streamline operations and limit risk exposure. From day one,… more
    Grant Thornton LLP (09/07/24)
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  • Equity Research - Gaming and Lodging…

    JPMorgan Chase (New York, NY)
    …triangulating data, and solving puzzles? You have found the right team! As an Associate in Equity Research covering Gaming and Lodging, you will become an ... conduct and facilitate industry analysis and company-specific coverage. **Job Summary** As an Associate in Equity Research - Gaming and Lodging, you will become… more
    JPMorgan Chase (08/01/24)
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  • Regulatory Associate , In-Business…

    City National Bank (New York, NY)
    ** REGULATORY ASSOCIATE , IN-BUSINESS CLIENT SERVICE & OPERATIONS RISK & CONTROLS** **WHAT IS THE OPPORTUNITY?** This position will work directly with the City ... to support and assist in identifying, monitoring and mitigating operational and regulatory risks within Client Service & Operations.The role will support corporate… more
    City National Bank (08/22/24)
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  • Postdoctoral Research Associate

    New York Genome Center (New York, NY)
    …Genome Center (NYGC) are looking for a motivated individual to work as a Postdoctoral Research Associate within a highly creative and dynamic research team ... We are interested in developing computational and experimental tools to map the regulatory wiring of the chromatin to interrogate the regulatory variation… more
    New York Genome Center (07/01/24)
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  • Postdoctoral Research Associate

    New York Genome Center (New York, NY)
    …Center are looking for an energetic and motivated individual to work as a Postdoctoral Research Associate within a highly creative and dynamic research team ... evolution. The lab is committed to translating clinically relevant basic research findings into genomic diagnostics and incorporating these into precision cancer… more
    New York Genome Center (08/11/24)
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  • Associate Director, Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary This position ... serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational...may serve as an ad hoc member of Global Project Team (GPT) to address labeling issues for late… more
    Daiichi Sankyo Inc. (07/01/24)
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  • Associate Research Fellow, Anti

    Pfizer (Pearl River, NY)
    …discovery and development. The role will be in close alignment with colleagues within the research unit as well as project teams and partner lines to inform ... and therapeutics. + Communicate analyses and study findings with internal project teams, leadership, and external collaborators. Publish research findings… more
    Pfizer (09/06/24)
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  • Associate Principal Scientist, Biologics…

    Merck (Rahway, NJ)
    Associate Principal Scientist position available at its Kenilworth, New Jersey research facility. The Associate Principal Scientist is a laboratory-based ... **Job Description** Our Research Scientists are our Inventors. We identify and...+ Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.… more
    Merck (09/12/24)
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  • Senior Clinical Research Associate

    IQVIA (New York, NY)
    IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (06/28/24)
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  • Clinical Research Associate

    IQVIA (Parsippany, NJ)
    **Role Overview:** As a Clinical Research Associate , you'll be at the forefront of ensuring our study sites operate smoothly and efficiently. Your work will be ... pivotal in advancing groundbreaking research . **Key Responsibilities:** + **Site Visits:** Conduct selection, initiation,...with sites to develop and track recruitment plans, ensuring project needs are met. + **Training & Communication:** Provide… more
    IQVIA (07/24/24)
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  • Postdoctoral Research Associate

    New York Genome Center (New York, NY)
    …expression and phenotypes at the cellular, tissue and physiological levels. The specific project would be tailored according to the interests and expertise of the ... postdoc, but possible projects include developmental GTEx (https://dgtex.org/) , regulatory variant mapping and characterization large single-cell data from T cells,… more
    New York Genome Center (07/12/24)
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  • Clinical Research Associate

    IQVIA (Parsippany, NJ)
    …experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (08/20/24)
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  • (Senior) Clinical Research Associate

    IQVIA (Parsippany, NJ)
    …degree. * In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice (GCP) and International ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (07/31/24)
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  • Oncology Clinical Research Associate

    IQVIA (Linden, NJ)
    …of degree. * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice (GCP) and International ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (09/04/24)
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  • Associate Director, Project

    Merck (Rahway, NJ)
    Research & Division organization of our company. **Position Description/Summary:** The GPAM Associate Director, Project Manager, is a core member of Early ... Company's drug and vaccine development efforts to progress the Research & Development pipeline and realize its full potential....& Development pipeline and realize its full potential. The Associate Director is expected to provide project more
    Merck (09/13/24)
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