• Clinical Trial Disclosure (CTD)…

    University of Miami (Coral Gables, FL)
    …requirements for clinical trials disclosure. The CTD Associate reports to the Sr . Clinical Trial Disclosure Associate . The objective is to ... tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . CORE JOB SUMMARY ​ The Clinical Trial Disclosure Associate within… more
    University of Miami (09/24/25)
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  • Sr . Clinical Research…

    ICON Clinical Research (Naperville, IL)
    Senior Clinical Research Associate ...Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + ... clinical development. We are currently seeking a Senior Clinical Research Associate (CRA)...will play a critical role in overseeing and managing clinical trial activities to ensure they are… more
    ICON Clinical Research (09/20/25)
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  • Associate Director, TAIP Principal Analyst…

    Bristol Myers Squibb (Princeton, NJ)
    …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... . **Position Summary** The TAIP Principal Analyst is a mid- senior level role within Bristol Myers Squibb's Trial...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… more
    Bristol Myers Squibb (09/29/25)
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  • Sr . Research Associate 3 - Urology

    University of Miami (Miami, FL)
    …JAMA Oncol. 2020;6(4):e196496). We are currently evaluating this biomarker in an active clinical trial and are pursuing similar mechanisms and developing new ... Urology has an exciting opportunity for a full time Sr . Research Associate 3, SOM to work...research program is to define the underlying biochemical and clinical behavior of prostate, kidney, and bladder cancers in… more
    University of Miami (09/17/25)
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  • Sr . Principal Associate Quality…

    Lilly (Lebanon, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Sr . Principal Associate Quality Excellence and Inspection Readiness is responsible for partnering with the Compliance Leader to provide technical… more
    Lilly (09/12/25)
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  • Sr . Research Associate 3

    University of Miami (Miami, FL)
    …institutional guidelines, tissue dissection, primary tissue culture. Assists in Phase I clinical trial related sample receipt, handling and documentation with ... SCCC has an exciting opportunity for a Full Time Sr . Research Associate 3 to work at...of our lab is to generate preclinical data for clinical translation. Relevant experience in immunology, cell biology, molecular… more
    University of Miami (08/08/25)
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  • Sr Administrative Services Associate

    Penn Medicine (Philadelphia, PA)
    …shape our future each day. Are you living your life's work? Job Title: Sr Administrative Services Associate Department: EPS Lab Location: Hospital of the ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
    Penn Medicine (08/07/25)
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  • Sr Administrative Services Associate

    Penn Medicine (Philadelphia, PA)
    …our future each day. Are you living your life's work? Job Title: Sr Administrative Services Associate Department: Otorhinolaryngology Location: Hospital of the ... Working for this leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today at Penn… more
    Penn Medicine (08/07/25)
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  • Sr . Principal Associate

    Lilly (Indianapolis, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Sr . Principal Associate for Analytical Quality Assurance ensures that laboratory activities conducted in the Lilly Medicine Foundry and with external… more
    Lilly (09/18/25)
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  • Sr . CRA, Sponsor Aligned, Oncology

    IQVIA (Overland Park, KS)
    …Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
    IQVIA (08/08/25)
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