• Clinical Research Manager - JJMT…

    J&J Family of Companies (Irvine, CA)
    …and strategic business needs + Manages work independently solves problems arising during clinical trial execution, and will seek guidance for more complex ... required + Previous experience in managing or supervising global clinical trials + A minimum of 2...Medical Device experience is required. + Sound knowledge ofICH-GCP, Clinical trial procedures **Preferred Education & Skills/Experience:**… more
    J&J Family of Companies (11/22/25)
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  • Senior Director, Head of Global Clinical

    BeOne Medicines (San Mateo, CA)
    …Process Owners (GPOs) to shape and execute a continuous improvement plan for end-to-end clinical trial processes owned by Global Clinical Operations. This ... including regional considerations to ensure the organization can seamlessly execute global clinical trials across multiple indications in Oncology. You will also… more
    BeOne Medicines (11/20/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. ... reports, and track resolution of action items. + Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol,… more
    Abbott (11/18/25)
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  • Clinical Site Lead - Los Angeles

    Abbott (Pleasanton, CA)
    …knowledge, procedure support (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and clinical research ... technical expertise to train site and Abbott staff for clinical trials and applicable commercial launches. +...needed, provide clinical and technical expertise for clinical trial procedure support + Attend study… more
    Abbott (11/01/25)
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  • Global Clinical Supply Chain Leader

    Genentech (South San Francisco, CA)
    …You will work closely with stakeholders to align supply chain strategies with clinical trial milestones, ensuring continuous and patient-centric delivery of IMP. ... in demand planning, supply optimization, and regulatory compliance to support impactful clinical trials . **The Opportunity** + You will manage demand and… more
    Genentech (10/16/25)
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  • Psychometric Clinical Rater

    System One (Ozark, MO)
    …disorders as part of the required study assessments for subjects participating in a clinical trial . The Clinical Rater will have excellent interpersonal, ... + Perform psychiatric diagnostic interviews and psychometric testing as part of clinical trial evaluations. + Collaborates with principal investigators, research… more
    System One (10/09/25)
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  • Director - Clinical Affairs

    Caldera Medical (Westlake Village, CA)
    …with Good Clinical Practice (GCP), ISO 14155, and local/international clinical trial regulations. * Develop strategies for peer-reviewed publications, ... compliance with Good Clinical Practice (GCP), ISO 14155, and local/international clinical trial regulations. Required Knowledge, Skills and Abilities: * BS… more
    Caldera Medical (10/02/25)
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  • Clinical Research Coordinator

    Actalent (Newark, NJ)
    Clinical Research Coordinator to facilitate the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various ... protocols and guidelines. Responsibilities + Coordinate the initiation and activation of clinical trial protocols, ensuring all necessary approvals are in place.… more
    Actalent (11/20/25)
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  • Clinical Programmer, Integrated Data…

    J&J Family of Companies (Titusville, NJ)
    …**Preferred Skills:** Advanced Analytics, Analytical Reasoning, Biological Sciences, Biostatistics, Clinical Trials , Data Modeling, Data Privacy Standards, Data ... Innovative Medicine is searching for the best talent for the position of ** Clinical Programmer** to join our Integrated Data Analytics and Reporting team (IDAR).… more
    J&J Family of Companies (11/13/25)
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  • Senior Clinical Research Associate

    ICON Clinical Research (Blue Bell, PA)
    …this role, you will be a key contributor to the successful execution of clinical trials , ensuring studies are conducted in full alignment with protocols, ... Doing:** + Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials . + Ensuring protocol compliance, data integrity, and… more
    ICON Clinical Research (10/16/25)
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