• Associate Director - Copyright…

    Lilly (Indianapolis, IN)
    …new medicines that will help solve our world's greatest health challenges. The Associate Director -Copyright and Translation role is accountable for the final ... data collection instruments (English/Translations) used in clinical trials. The C/T associate director also provides guidance on linguistic validations,… more
    Lilly (02/21/25)
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  • Associate Director , Clinical Trial…

    Lilly (Indianapolis, IN)
    …better for people around the world. The Clinical Trial (CT) Supply Chain Associate Director will provide operational leadership of clinical supply chain data, ... review, and/or approve appropriate documents outlined in business processes. o Maintain GMP/ GCP compliance . o Reach across boundaries and integrate information… more
    Lilly (03/19/25)
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  • Associate Clinical Project Management…

    IQVIA (Avon, IN)
    …delivery, ensuring consistent use of study tools and training materials and compliance with system updates, standard processes, policies and procedures. * Serve as ... and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial… more
    IQVIA (03/06/25)
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