• Clinical Research Associate II - Smidt…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Nurse, or Principal Investigator to coordinate/implement study. *Evaluates and abstracts clinical research data from source documents. *Completes Case Report… more
    Cedars-Sinai (07/16/25)
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  • Clinical Research Associate I,…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Administrator or Research Nurse to coordinate/implement study. + Evaluates and abstracts clinical research data from source documents. + Ensures compliance with… more
    Cedars-Sinai (08/30/25)
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  • Bilingual Clinical Research Associate I…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Administrator or Research Nurse to coordinate/implement study. + Evaluates and abstracts clinical research data from source documents. + Ensures compliance with… more
    Cedars-Sinai (08/01/25)
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  • Clinical Research Associate I- Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Administrator or Research Nurse to coordinate/implement study. *Evaluates and abstracts clinical research data from source documents. *Ensures compliance with… more
    Cedars-Sinai (07/16/25)
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  • Heart Institute Clinical Research Assoc…

    Cedars-Sinai (Los Angeles, CA)
    …the coordination/implementation of noncomplex research studies. + Collects, evaluates and/or abstracts clinical research data . May assist in designing forms for ... data collection/abstraction. Enters and processes clinical research data into Electronic ...the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical more
    Cedars-Sinai (07/02/25)
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  • Director, Early Clinical Development…

    Bristol Myers Squibb (Brisbane, CA)
    …Articulating clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal ... lives. Read more: careers.bms.com/working-with-us . **Job Title** Director, Early Clinical Development - Immunology **Functional Area Description** The Early … more
    Bristol Myers Squibb (08/12/25)
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  • Biomedical Data Stewardship Senior Manager

    Amgen (Thousand Oaks, CA)
    …their use in coordination with assigned subject matter experts. + Lead the design and review clinical data quality edit checks aligned with CRF content. + ... Stewardship Manager to drive the design, implementation, and governance of standardized data collection practices across our clinical programs. In this vital… more
    Amgen (06/27/25)
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  • Senior Director, Clinical Development,…

    BeOne Medicines (Emeryville, CA)
    …from sites, IRBs/IECs, Health Authorities, and CROs + Review , query, and analyze clinical trial data + Interpret, and present clinical trial data ... The Senior Director, Clinical Development, Solid Tumors will support BeOne ...the Job:** + Facilitate generation of, author, update, and/or review key documents, including, but not limited to: +… more
    BeOne Medicines (08/30/25)
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  • Director, Clinical Development, Solid…

    BeOne Medicines (San Mateo, CA)
    …from sites, IRBs/IECs, Health Authorities, and CRO's + Review , query, and analyze clinical trial data . + Interpret, and present clinical trial data ... The Director, Clinical Development will support BeOne Clinical ...the Job:** + Facilitate generation of, author, update, and/or review key documents, including, but not limited to: +… more
    BeOne Medicines (07/24/25)
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  • Executive Director, Clinical Development,…

    BeOne Medicines (San Mateo, CA)
    …from sites, IRBs/IECs, Health Authorities, and CROs + Review , query, and analyze clinical trial data + Interpret, and present clinical trial data ... The Executive Director, Clinical I/O Development will support BeOne Medicine's ...the job:** + Facilitate generation of, author, update, and/or review key documents + Protocol concepts, synopses, protocols, and… more
    BeOne Medicines (07/19/25)
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