• Senior Field Specialist, Clinical Research…

    Cordis (Irvine, CA)
    …working directly with physicians and healthcare professionals + Prior experience with clinical trials (preferred) + Experience in coronary or peripheral ... the site for communication with SELUTION CSM, CRA, and CRO team + Partner with SELUTION clinical ...Ability to travel (at least 75%) to company and clinical trial sites Pay / Compensation The… more
    Cordis (08/13/25)
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  • Clinical Research Associate ll

    Abbott (Alameda, CA)
    …Participate in cross-functional clinical team(s) in the planning and execution of clinical trials . + Proactively and effectively communicate the status of ... members, peers, and management. + Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical more
    Abbott (08/08/25)
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  • Clinical Research Associate, Coronary…

    Cordis (Irvine, CA)
    … study team in the coronary space to execute a randomized, multi-center IDE clinical trial . You will perform various duties and responsibilities as directed by ... assist in organizing and monitoring the different stages of clinical trials . You will interact with healthcare...and applicable local regulations + Manage and maintain internal Trial Master Files (TMFs). Potentially develop a standardized eTMF… more
    Cordis (07/11/25)
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  • Senior Director, Clinical Development,…

    BeOne Medicines (Emeryville, CA)
    clinical protocol + Provide scientific and medical support throughout conduct of a clinical trial ; respond to clinical questions from sites, IRBs/IECs, ... Health Authorities, and CROs + Review, query, and analyze clinical trial data + Interpret, and present...program is essential, including involvement in all stages of clinical trials (ie from start up to… more
    BeOne Medicines (08/30/25)
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  • Lead- Clinical Data Management

    J&J Family of Companies (Irvine, CA)
    …with data cleaning and quality review processes for assigned projects. S/he ensures clinical trial data collected meet the highest standards of data integrity, ... management processes and procedures + Independently lead several complex trials + Lead CRF design, review and validation of... + Lead CRF design, review and validation of clinical database, including management of CRO activities… more
    J&J Family of Companies (09/03/25)
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  • Associate Vice President, Clinical Data…

    Amgen (Thousand Oaks, CA)
    …strategic direction, leadership, and operational oversight of data management processes supporting clinical trials across all therapeutic areas and phases. This ... compliance, and strategic leadership within a pharmaceutical, biotech, or CRO environment. + Expertise in GCP, ICH, FDA, EMA...in GCP, ICH, FDA, EMA regulations, data governance, and clinical trial data standards (CDISC, SDTM). +… more
    Amgen (08/14/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …with CRAs to ensure data collection is met per contractual guidelines * Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to ... Familiar with industry CTMS and data management systems **Other Qualifications:** * Understands clinical trial processes with a thorough knowledge of ICH and… more
    BeOne Medicines (07/23/25)
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  • Associate Director, Neuroscience, Clinical

    Bristol Myers Squibb (San Diego, CA)
    …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial /biomarkers and asset development as well as ... drug development and activities required for and related to clinical trial initiation, maintenance and completion +...perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of… more
    Bristol Myers Squibb (07/24/25)
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  • Principal Scientist, Clinical Research

    Unilever (El Segundo, CA)
    …Execute robust clinical trial pipeline + Support strategy for future clinical trials + Conduct thorough literature reviews on a wide variety of hydration ... in any way modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision. Ability to competently perform all the… more
    Unilever (08/14/25)
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  • Executive Director, Clinical Development,…

    BeOne Medicines (San Mateo, CA)
    clinical protocol + Provide scientific and medical support throughout conduct of a clinical trial ; respond to clinical questions from sites, IRBs/IECs, ... selection of investigator and vendors + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic...Health Authorities, and CROs + Review, query, and analyze clinical trial data + Interpret, and present… more
    BeOne Medicines (07/19/25)
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