• Clinical Research Associate

    Translational Research in Oncology (Los Angeles, CA)
    If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO ... query resolution in a timely manner to ensure clean data availability for studies analyses + Input and maintain...Project Management Departments + Oversee study drug management at clinical study sites (availability, receipt,… more
    Translational Research in Oncology (08/22/25)
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  • Clinical Assistant/ Associate

    Kean University (Union, NJ)
    …Health Professions and Human Services, Department of Nursing** **Nursing (12 Month Clinical Assistant/ Associate Professor) -** the Clinical tenure-track ... fields - you will need to verify that the data is accurate.** **In the "My Experience" section, you...six colleges - the College of Business and Public Management ; the College of Education; the College of Liberal… more
    Kean University (09/11/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (San Mateo, CA)
    …PowerPoint and Outlook * Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a ... is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient… more
    BeOne Medicines (09/17/25)
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  • Clinical Research Associate

    IQVIA (Durham, NC)
    IQVIA is hiring a Clinical Research Associate with on-site monitoring experience in GLP-1/Obesity/Diabetes (Type II) clinical trials. Phase 1 experience is a ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...* If applicable, may be accountable for site financial management according to executed clinical trial agreement… more
    IQVIA (07/04/25)
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  • Senior Data Management

    Merck (Lower Gwynedd, PA)
    **Job Description** **Job Description** Data Management Associate (P3), Regulated Bioanalytics, Regulated Robotics & Data , LIMS & Data Management ... The PDMB Regulated Bioanalytics Department is seeking a Data Management Associate to join...will be utilized to generate pivotal safety and efficacy clinical patient data required for regulatory filings.… more
    Merck (09/16/25)
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  • Clinical Research Coordinator…

    Stanford University (Stanford, CA)
    …+ Interact with lead biostatistician regularly, ensuring proper study implementation and data management . + Meet with PI and research manager regularly ... Clinical Research Coordinator Associate (1 Year...and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research… more
    Stanford University (09/13/25)
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  • Associate Clinical Scientist, Cell…

    Bristol Myers Squibb (Princeton, NJ)
    data collection in alignment with the protocol in collaboration wi th Data Management /Programming **Degree Requirements** + Degree in Life Sciences (MD, PhD, ... and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Scientist function provides scientific expertise necessary to design and… more
    Bristol Myers Squibb (09/28/25)
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  • Clinical Associate

    Abbott (Dallas, TX)
    …generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ** Clinical Associate ** **About Abbott** Abbott is a global healthcare leader, ... monitors performance and reports status to manager. As a Clinical Associate on the US Abbott EP...personnel; + Facilitating regional training seminars; + Participating in clinical studies/ data collection; + Troubleshooting; and, +… more
    Abbott (09/27/25)
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  • Associate Director, Strategic Sourcing,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …categories including data management , diagnostics, patient platforms, site management and clinical trial support suppliers across all phases of ... The Associate Director, Strategic Sourcing, Clinical Category...to meet regulatory requirements (ie J-sox, Third Party Risk Management , etc.). + Ensures best practices in Sourcing including… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    …and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management , adverse event management to ... Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory...clinical team and report as required. + Enter data on Hematology, Oncology and Stem Cell Transplant patients… more
    Touro University (07/24/25)
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