• Bilingual Clinical Research Associate I - Ramin…

    Cedars-Sinai (Los Angeles, CA)
    …or patient contact for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of ... for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for… more
    Cedars-Sinai (08/01/25)
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  • Clinical Research Associate I, Tan Lab

    Cedars-Sinai (Los Angeles, CA)
    …or patient contact for long term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of ... for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for… more
    Cedars-Sinai (07/16/25)
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  • Clinical Research Associate I- Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …or patient contact for long term follow-up patients only. *Assists with regulatory submissions to the Institutional Review Board (IRB) including submission ... for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for… more
    Cedars-Sinai (07/16/25)
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  • Executive Medical Director, Clinical Development

    Taiho Oncology (Pleasanton, CA)
    …within the global development program(s) + Answer medical questions raised by Regulatory Agencies (RA) and Institutional Review Boards/ Ethics Committees ... all clinical questions related to the development program. + Perform data review supported by Clinical Research Scientist(s) (CRS), participate in protocol deviation… more
    Taiho Oncology (06/25/25)
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  • Scientist, Purification Process Development…

    Gilead Sciences, Inc. (Foster City, CA)
    …documentation (development reports, process description, batch records, etc) Author and review CMC related regulatory sections Demonstrates technical proficiency ... for purification technology development, platform process evolution, and support of regulatory filings. We are seeking a highly motivated, team-oriented individual… more
    Gilead Sciences, Inc. (06/14/25)
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  • Pharmacovigilance Specialist

    Grifols Shared Services North America, Inc (Los Angeles, CA)
    …Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data review , compilation and ... Serves in an advisory capacity including activities such as product monographs review ; draft responses to pharmacovigilance requests from regulatory agencies;… more
    Grifols Shared Services North America, Inc (06/03/25)
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  • Clinical Documentation Improvement (CDI)…

    Guidehouse (Escondido, CA)
    …of mortality for the patient and is reflective of current CMS or other regulatory standards. + Conducts daily, concurrent review of inpatient records on assigned ... Communicates to the CDI Coordinator when volume of daily review assignments is too high or low so that...low so that CDI Coordinator can assist in adjusting review assignments amongst the team. + Initiates compliant physician… more
    Guidehouse (07/25/25)
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  • Clinical Research Coordinator I (Part-Time)…

    Cedars-Sinai (Santa Monica, CA)
    …information at regular research staff meetings. + Works closely with investigators and regulatory staff or directly with Institutional Review Board (IRB) to ... to successfully implement research protocols, in compliance with all regulatory requirements. **Primary Duties and Responsibilities:** + Responsible for… more
    Cedars-Sinai (08/14/25)
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  • Director, Clinical Data Science (Biostatistician)

    J&J Family of Companies (Irvine, CA)
    …oversight activities for Biostatistics, Programming and Data Management + Interact with regulatory agencies to support the review process of statistical ... verbal and written communication skills required. + Experience interacting with regulatory agencies required. + Experience programming with SAS or R required.… more
    J&J Family of Companies (07/25/25)
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  • Mid-Level Facilities Mechanical HVAC Engineer

    The Boeing Company (El Segundo, CA)
    …support to construction projects as needed (vendor selection, contractor proposal review , interface with regulatory agencies, etc.) + Prepare contingency ... identify errors and document construction changes to comply with regulatory requirements, facility standards, and record retention + Provide technical… more
    The Boeing Company (07/21/25)
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