• Senior Clinical Research Monitor,…

    Edwards Lifesciences (Indianapolis, IN)
    …lives. Join us and be part of our inspiring journey. As the Senior Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are ... for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters...+ Clinical research certification (ACRP or SOCRA, Clinical Coordinator /CRA certification) + Prior clinical more
    Edwards Lifesciences (02/10/24)
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  • Senior Clinical Research Monitor,…

    Edwards Lifesciences (Indianapolis, IN)
    …lives. Join us and be part of our inspiring journey. As the Senior Clinical Research Monitor, you will ensure trial patients' safety by assuring trials are ... for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters...+ Clinical research certification (ACRP or SOCRA, Clinical Coordinator /CRA certification) + Prior clinical more
    Edwards Lifesciences (02/03/24)
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  • Associate Director, Clinical Quality…

    Merck (Indianapolis, IN)
    …The CQOM will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area, to proactively embed ... Categorization Tools and Quality Plans in partnership with the Clinical Trial Team (CTT). + Collectively and...inspection, worldwide. + In collaboration with the Global Inspection Coordinator and Head of CQO, maintain and QC the… more
    Merck (04/24/24)
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