• Associate Director - Clinical Development,…

    Lilly (Indianapolis, IN)
    trial process. **Scope -** Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make adjustments and ... and integrating inputs across functions and geographies. **Risk** - Assess, identify and monitor trial -level risks. Incorporate knowledge, trial process, and… more
    Lilly (05/07/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Indianapolis, IN)
    …execute corporate clinical strategy for global development projects in Oncology + Monitor clinical trial progress, identify and mitigate risks, and make ... from preclinical experiments to the end of the product's life cycle. + Clinical Trial Oversight: Develop and oversee clinical trial strategies, ensuring… more
    Sumitomo Pharma (05/15/25)
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  • Associate Director- Clinical Trial

    Lilly (Indianapolis, IN)
    …are determined to make life better for people around the world. Associate Director- Clinical Trial Foundations Purpose: The Associate Director, Clinical ... Trial Foundations (CTF), will serve as the subject matter expert for clinical systems and capabilities supporting clinical development. In this role, you will… more
    Lilly (05/21/25)
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  • Clinical Laboratory Sciences Apprentice…

    Lilly (Indianapolis, IN)
    …purpose of the CLS Specialist is to serve a pivotal role in the creation of a clinical trial laboratory database, tracking of clinical trial samples from ... as well as the results delivery associated with those clinical trial samples. This includes ensuring the...Create and utilize dashboards to report our metrics to clinical teams and leadership + Monitor for… more
    Lilly (05/21/25)
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  • IT Product Manager - Clinical Systems

    Lilly (Indianapolis, IN)
    …Vision** - Develop and implement the landscape vision, strategy, and roadmap for clinical trial product delivery technology, in alignment with the company's ... business value. **External Sensing** - Provide thought leadership and expertise on clinical trial supply technology trends, best practices, and standards, and… more
    Lilly (03/28/25)
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  • Associate Director - CTF Clinical Results…

    Lilly (Indianapolis, IN)
    …world. Purpose: The Associate Director, CTF Clinical Results Systems (as part of Clinical Trial Foundations) is a leader and key partner across the business. ... processes and technology ▪ Knowledge of emerging IT capabilities used for clinical trial data management ▪ Capacity and workload management expertise… more
    Lilly (05/17/25)
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  • Clinical Research Specialist

    Community Health Network (Indianapolis, IN)
    …investigators in identifying, screening, interviewing, and consenting eligible patients for the clinical trial and completing the associated data entry and ... Clinical Research Specialist Job Ref 2502284 Category Administrative...regulations as needed and as trained + Participates in monitor and regulatory audits and routine department meetings as… more
    Community Health Network (04/11/25)
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  • Field Clinical Manager - MItral & Tricupsid…

    Medtronic (IN)
    …+ Manage and direct the daily operations of the Therapy Development team for clinical trial case support, executing on the strategies outlined by the Director, ... with a cross functional team including Research and Development, Clinical , Quality, and others to ensure therapy adoption by...support to ensure safe adoption and procedural outcomes. + Monitor , guide, and coach remote direct reports to achieve… more
    Medtronic (05/28/25)
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  • Medical Director

    Grifols Shared Services North America, Inc (South Bend, IN)
    …safety data (toxicology) and use this information to develop safety mitigation strategies in clinical trial design + Serve as a key part of the cross-functional ... in collaboration with the contract research organization (CRO) medical monitor , or directly with study investigators + Work closely... rsearch experience with at least 5 years of clinical document production and/or clinical trial more
    Grifols Shared Services North America, Inc (05/30/25)
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  • Materials Planner

    Catalent Pharma Solutions (Greendale, IN)
    …for managing all material related Planning activities needed to meet trial , commercial, and process development manufacturing requirements. The principal objective ... Role** + Write purchase orders in system and send to suppliers based on Trial Production schedule, purchase requisitions, and forecast files. + Execute / monitor more
    Catalent Pharma Solutions (05/16/25)
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