• Senior Principal Scientist, Clinical

    Abbott (Sylmar, CA)
    …provide directives to teams as well as study sites. Be able to mentor other clinical scientists within Clinical Research . **What You'll Work On** + Provide ... treat people with heart arrhythmias, or irregular heartbeats. **Senior** **Principal** ** Clinical ** ** Research ** **Scien** **tist** **,** will be viewed as… more
    Abbott (08/08/25)
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  • Senior Clinical Research Scientist

    Danaher Corporation (Sunnyvale, CA)
    …System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Clinical Research Scientist reporting to the ... Director, Clinical Research , develops and independently writes clinical documentation...content of clinical study reports and review clinical and analytical sections for regulatory submissions… more
    Danaher Corporation (06/11/25)
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  • Clinical Research Associate ll

    Abbott (Alameda, CA)
    …+ BS degree in life sciences or equivalent with minimum 5 years of clinical research experience + Must have 2+ years of relevant experience in ... clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical ...flexible when priorities change. + Working knowledge of GCP, Clinical and Regulatory Affairs. + Proficient with… more
    Abbott (08/08/25)
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  • Senior Principal Clinical Research

    GRAIL (Menlo Park, CA)
    Clinical Operations, Biostatistics, Clinical Data Management, Medical Affairs, Regulatory Affairs, Research and others. This role will provide strategic ... formal networks with external investigators and thought leaders to support clinical study programsEnsure compliance with industry regulations, policies,… more
    GRAIL (09/06/25)
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  • Clinical Research Coordinator

    Actalent (Merced, CA)
    …reporting. Process laboratory specimens per study requirements. Qualifications 3-5 years of Clinical Research Coordinator Experience with clinical ... and key stakeholders to plan, coordinate, implement, and complete clinical trials and research projects. You will...in collaboration with the PI and healthcare team. Ensure compliance with study protocols, regulatory requirements, and… more
    Actalent (09/03/25)
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  • Clinical Research Associate…

    ICON Clinical Research (CA)
    As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... work in United States without visa sponsorship + A clinical research professional with 2+ years of...areas, including Immunology preferred. + Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS… more
    ICON Clinical Research (08/28/25)
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  • Associate General Counsel, Senior Director…

    Oura (San Francisco, CA)
    …evolving regulatory guidance and guide teams on risk-based approaches to regulatory compliance in product development, clinical validation, and market ... at local co-working locations. The AGC, Senior Director of Regulatory Compliance & Privacy will provide strategic...and health and wellness claims. + Provide legal and regulatory oversight for clinical studies and evidence… more
    Oura (08/17/25)
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  • Clinical Research Coordinator

    Actalent (San Diego, CA)
    …and federal regulatory guidelines. Oversee the quality of the medical and clinical research data. Provide direction and guidance to investigators. Assist PIs ... and a Bachelor's degree in related area + Demonstrated experience in clinical trials research . Strong knowledge of experimental protocols, data gathering,… more
    Actalent (09/06/25)
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  • Clinical Research Nurse

    Actalent (Santa Maria, CA)
    …Principal Investigators, and key stakeholders to plan, coordinate, implement, and complete clinical trials and research projects. You will oversee complex ... patient care, and serve as a role model for research nursing excellence. Key Responsibilities + Oversee and manage...collaboration with the PI and healthcare team. + Ensure compliance with study protocols, regulatory requirements, and… more
    Actalent (09/03/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …and/or medical devices * Conduct site visits to determine protocol and regulatory compliance , and prepare required documentation * Develop collaborative ... responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient...processes with a thorough knowledge of ICH and associated regulatory guidelines * Minimum of 4-6 years of relevant… more
    BeOne Medicines (07/23/25)
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