• Research Project Associate

    Memorial Sloan-Kettering Cancer Center (New York, NY)
    …Description Exciting opportunity at MSK: Join our team as aResearch Project Associate ! We're looking for a dynamic clinical research professional to support ... determined by management. Key Qualifications: + 2-4 years of Clinical Research / Project Management experience. + 1-2 years of regulatory experience, 2+ years… more
    Memorial Sloan-Kettering Cancer Center (10/24/24)
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  • Associate Director - Global…

    Novo Nordisk (Plainsboro, NJ)
    …reports, preclinical reports, investigator brochures, application summary documents, etc. + Research and analyze the evolving competitive and regulatory ... in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
    Novo Nordisk (09/17/24)
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  • Regulatory Associate , Portfolio…

    City National Bank (New York, NY)
    ** REGULATORY ASSOCIATE , PORTFOLIO MANAGEMENT RISK AND CONTROL** **WHAT IS THE OPPORTUNITY?** This position will work directly with the City National Rochdale's ... to support and assist in identifying, monitoring and mitigating operational and regulatory risks within Portfolio Management Risk and Control.The role will support… more
    City National Bank (09/27/24)
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  • Equity Research - Media - Associate

    JPMorgan Chase (New York, NY)
    As an Associate in Equity Research covering Media, you will become an industry expert, helping to conduct and facilitate industry analysis and company-specific ... puzzles? You have found the right team! As an Associate in Equity Research - Media, you...facilitate industry analysis and company-specific coverage. This involves core research ranging from dissecting earnings releases and regulatory more
    JPMorgan Chase (10/10/24)
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  • Clinical Research Associate I…

    Mount Sinai Health System (New York, NY)
    **Job Description** The Clinical Research Associate is an integral part of the research study team and monitors all safety aspects of clinical research ... clinical studies as a clinical trial assistant or clinical research associate is required. + Excellent Communication...findings in a summary format to the Director of Research and Quality Outcomes. + Interfaces with project more
    Mount Sinai Health System (10/23/24)
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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 (09/30/24)
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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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  • 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 (10/11/24)
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  • Clinical Research Associate III…

    WuXi AppTec (Cranbury, NJ)
    **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... query management and data audit functions. + Performs other project -related duties as specified by project manager...supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II personnel.… more
    WuXi AppTec (08/31/24)
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  • Associate Director Project

    WuXi AppTec (Cranbury, NJ)
    …manufacturing and/or Drug Product R&D and manufacturing. + Prior experience in project management or managing external research collaborations, with PMP ... **Overview** WuXi TIDES, a leading Contract Research and Development Manufacturing Organization (CRDMO), is an...development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC… more
    WuXi AppTec (10/18/24)
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  • Associate Director, Clinical Supply…

    Merck (Rahway, NJ)
    …the 'end-to-end' integrated clinical supply chain across the full company Research Laboratories ( Research and Development Division) portfolio of clinical ... and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the primary program-level GCS point… more
    Merck (10/12/24)
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  • Regulatory Planning Manager (Hybrid)

    RWJBarnabas Health (Somerset, NJ)
    …Facilities/Design, Standards and Operational leadership. Manager conducts internal and external research for regulatory standards and interpretations to assist ... should be in a closely related field such as health/business administration, regulatory compliance, accreditation or licensure associate , business development or… more
    RWJBarnabas Health (10/18/24)
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  • Director, Regulatory Reform and Customer…

    City of New York (New York, NY)
    …and a strong focus on its employees. The Director will manage the Regulatory Reform team within the Division of Business Services reporting to the Assistant ... Commissioner of Government Navigation and Regulatory Reform. The team's mission is to ensure that...strategic thinking to ensure success - Creating and communicating project plans, including identifying milestones and risks, to multiple… more
    City of New York (10/02/24)
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  • Associate Director, Tech Transfer Leader

    Merck (Rahway, NJ)
    …We are seeking a highly motivated individual for the role of Associate Director, Tech Transfer Leader in Large Molecule Technology Transfer within Technical ... Health, Process Development, Commercialization, Operations, Technical Operations, Analytical, Quality, Regulatory -CMC, and Supply Chain. The end-to-end scope includes Drug… more
    Merck (10/23/24)
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  • Associate Director, State Affairs (East)

    Cypress Creek Renewables (New York, NY)
    Associate Director, State Affairs (East) at Cypress Creek Renewables (View all jobs) (https://ccrenew.com/careers/) New York or East Coast Remote The Company Cypress ... Creek Renewables is powering a sustainable future, one project at a time. We develop, finance, own and...our infrastructure development by driv ing new legislative and regulatory policies , expand relationships with key stakeholders ,… more
    Cypress Creek Renewables (09/12/24)
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  • Associate Director High Performance…

    Mount Sinai Health System (New York, NY)
    …computing team, a research clinical data warehouse team and a research data services team. The Associate Director, High Performance Computational and ... with scientists to accelerate scientific discovery for basic and translational science research . To achieve these aims, we support a high-performance computing and… more
    Mount Sinai Health System (10/21/24)
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  • Quantitative Analytics Summer Associate

    JPMorgan Chase (New York, NY)
    …other functions including Risk, Finance, Model Risk & Development, Technology, and the Regulatory Capital Management Office. The models and research developed by ... **2025 Quantitative Analytics Associate Program - Summer Associate ** **Short...for MRGR operational processes, technology, review strategy and planning, project management of audits and regulatory commitments,… more
    JPMorgan Chase (10/16/24)
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  • Associate Principal Scientist, Engineering

    Merck (Rahway, NJ)
    …transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group ... pipeline of diverse products and evolving technologies. We are seeking an Associate Principal Scientist to advance and commercialize the intravitreal (IVT) pipeline… more
    Merck (10/23/24)
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  • Associate Director, Biostatistics

    Pfizer (New York, NY)
    …design, statistical analysis plans, interpretation and communication of statistical results, project development plans, regulatory issues, and scientific and ... clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. + Provide scientifically… more
    Pfizer (10/22/24)
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