• Executive Medical Director, Clinical

    Taiho Oncology (Pleasanton, CA)
    …investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents, and scientific ... + Use medical/scientific expertise and strategic thinking to develop clinical development plans (incl. study design and...publications. + Analyze and interpret outcome of clinical studies within the global development program(s)… more
    Taiho Oncology (06/25/25)
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  • Director, Clinical Development…

    Gilead Sciences, Inc. (Foster City, CA)
    …Global Headquarters in Foster City, CA. **EXAMPLE RESPONSIBILITIES:** + Lead or support clinical trial protocol design, clinical study report development, ... trial data + Present scientific information at scientific conferences as well as clinical study investigator meetings. + Adhere to regulatory requirements of … more
    Gilead Sciences, Inc. (08/27/25)
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  • Sr. Director, Clinical Development (MD)-…

    Gilead Sciences, Inc. (Foster City, CA)
    …with experience in medical monitoring and addressing medical concerns that arise during clinical studies , experience leading study concept and protocol ... scientific and clinical leadership on activities including clinical development plan generation; clinical study...regulatory requirements and impact on development and execution of clinical studies + Strong oral and written… more
    Gilead Sciences, Inc. (07/24/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 26, 2025 Requisition # 106673 The Division ... of Life and Pediatric Palliative Care is seeking a Clinical Research Coordinator Associate to conduct clinical ...assignments. Independently manages significant and key aspects of large studies or all aspects of one or more small… more
    Stanford University (08/07/25)
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  • Assistant Clinical Research Coordinator

    Stanford University (Stanford, CA)
    …related to the collection of clinical data and/or the coordination of clinical studies . Dr. McLaughlin is an NIH-funded clinical investigator whose ... patients with complex endocrine diseases. The basic science and clinical studies that are carried out at...Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or… more
    Stanford University (09/04/25)
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  • Senior Clinical Data Manager

    GRAIL (Menlo Park, CA)
    …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to ... management activities for one or multiple diagnostic product development studies in support of GRAIL's robust clinical ... development pipeline. **Responsibilities:** + Work closely with GRAIL study team members to ensure that clinical more
    GRAIL (08/13/25)
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  • Clinical Research Coordinator

    IQVIA (Fountain Valley, CA)
    …to **ECG, sample collection including spirometry, and vital signs.** + Coordinate clinical research studies conducted by a supervising principal investigator. + ... meetings with the project team as needed. + Performing clinical set-up and preparation for the study ...Performing clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting… more
    IQVIA (09/05/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …Precision Psychiatry and Neuroimaging to executeprecision medicine in mental health studies , The Clinical Research Coordinator Associate in Precision Psychiatry ... Clinical Research Coordinator Associate **School of Medicine, Stanford,...Coordinator Associate (CRCA) position is on a precision medicine study of depression funded by NIH under an exciting… more
    Stanford University (08/20/25)
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  • Clinical Research Associate

    Translational Research in Oncology (Los Angeles, CA)
    …be remote, but will require travel. Responsibilities: + Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory ... Visits, Routine Monitoring Visits and Site Close-out at assigned clinical study sites as per TRIO SOPs/SGs/IMs...a timely manner to ensure clean data availability for studies analyses + Input and maintain study more
    Translational Research in Oncology (08/22/25)
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  • Program Lead II, Clinical Program…

    AbbVie (San Francisco, CA)
    Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more ... clinical operational strategy and is responsible for the execution of clinical studies /programs (eg, generation of operational timelines, enrollment options,… more
    AbbVie (08/13/25)
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