• Trial Capabilities Associate

    Lilly (Indianapolis, IN)
    …location. The anticipated wage for this position is $63,000 - $140,800 **Purpose:** The Trial Capabilities Associate (TCA) provides clinical trial ... maintenance and close-out. The TCA may be assigned responsibilities within any trial capability, including obtaining clinical trial authorizations and ethics… more
    Lilly (01/08/25)
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  • Associate Director, CTF Product Owner,…

    Lilly (Indianapolis, IN)
    …and information to enable clinical development and speed medicines to patients. The Associate Director CTF Product Owner in Trial Management Systems will support ... wage for this position is $111,000 - $162,800 Purpose: Trial Management Systems as part of Clinical Trial...Technology and Process Implementation + System Owner for new capabilities which support drug development. + Drive the application… more
    Lilly (12/20/24)
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  • Associate Director - Clinical Trial

    Lilly (Indianapolis, IN)
    …solutions to support communities through philanthropy and volunteerism. **Purpose** : The Associate Director - Clinical Trial Foundations (CTF), will serve as ... collection systems, primarily focused on EDC and data aggregation systems. The Associate Director is responsible for collaborating with business partners to enable… more
    Lilly (12/27/24)
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  • Associate Director - eSource…

    Lilly (Indianapolis, IN)
    …(CDDA) provides leadership in the strategy and development of contemporary clinical trial processes, technologies, information, and capabilities and in shaping ... should have extensive experience supporting data collection and aggregation systems. Clinical Trial Foundations as part of Clinical Design, Delivery & Analytics… more
    Lilly (11/28/24)
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  • Senior Associate Central Monitor, Risk

    Pfizer (Indianapolis, IN)
    …Monitor is responsible for ensuring the completeness, quality and integrity of clinical trial data in Pfizer's Risk Based Monitoring (RBM) ecosystem. The areas of ... quality processes to meet quality, timelines and deliverables. + Use clinical trial process experience to translate study risks into technical specifications that… more
    Pfizer (01/05/25)
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  • Associate Regional Medical Scientific…

    Merck (Indianapolis, IN)
    **Job Description** **Job Description:** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease ... Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Associate Director's liaise between the scientific community and the Company… more
    Merck (01/07/25)
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  • US Scientific Director, Medical Affairs (SDMA)…

    Merck (Indianapolis, IN)
    …with organizational priorities. Along with the USMA Field Leaders (Executive Director (ED)/ Associate Vice President (AV)), the SDMA is responsible for regional FM ... of Medical Affairs (RDMA) (where applicable), US Global Clinical Trial Organization, Global Medical and Scientific Affairs (GMSA) TA...therapeutic and competitive landscape to optimize US FM Team capabilities + May be responsible for one or more… more
    Merck (01/08/25)
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