• AVP, Complex Claim Liability Specialist-Business…

    Travelers Insurance Company (Indianapolis, IN)
    …and resolve the company's most severe and/or complex Life Science medical products, clinical trial and pharmaceutical bodily injury claims, as well as General ... + CLAIM HANDLING: + Directly handle assigned severe/complex Life Science medical products, clinical trial and pharmaceutical bodily injury claims, as well as… more
    Travelers Insurance Company (05/03/25)
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  • Sr. Director - Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    …as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency ... Initiate andmaintainregulatorystrategydocuments byleveragingteam expertise, as well as scientific, drug/device clinical development and knowledgefromhealth authorities such as regulatory policies,… more
    Lilly (04/05/25)
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  • Senior Director Global Regulatory Lead (Early…

    Lilly (Indianapolis, IN)
    …as needed to inform development and manage issues. For preclinical and early clinical development programs, the GRL leads the US and Canada submissions and agency ... documents by leveraging team expertise, as well as scientific, drug/device clinical development and knowledge from health authorities such as regulatory policies,… more
    Lilly (03/27/25)
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  • Associate/Sr. Associate - Medicines Quality…

    Lilly (Indianapolis, IN)
    …in defined functional business areas, for example, medical writing, regulatory affairs, or clinical trial management. + Knowledge of quality systems + Ability to ... the Associate/Senior Associate/Principal Associate - MQO Portfolio is to support the clinical development and implementation of the strategy for GCP quality systems… more
    Lilly (05/16/25)
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  • Advisor/Sr. Advisor - GXP Risk Assessor, Audit…

    Lilly (Indianapolis, IN)
    …that have an impact on the fulfilment of Lilly's responsibilities as a clinical trial sponsor, medicine manufacturer and/or marketing authorization holder. + ... of internal and external quality audits related to pharmaceutical development, non- clinical and clinical research, and product commercialization. The role… more
    Lilly (05/27/25)
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  • Associate Director-Submission Data Delivery

    Lilly (Indianapolis, IN)
    …▪ Bachelor's degree ideally in a scientific area ▪ Minimum 5 years of clinical trial data experience in drug development in areas intersecting (eg ... for Statistics, Data and Analytics. ▪ Apply broad process/technology knowledge to ensure clinical trials are consistent and accurate ▪ Act as the main contact within… more
    Lilly (05/22/25)
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  • Senior Principal Scientist, Analytical Chemistry…

    Lilly (Indianapolis, IN)
    …and implementing robust analytical methods and control strategies to enable clinical trial material delivery and build process understanding. ... development of synthetic drug substances and drug products from the pre- clinical phase through commercialization. Our scientists and engineers develop innovative… more
    Lilly (05/31/25)
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  • Associate Director - Engineering and Computer…

    Lilly (Indianapolis, IN)
    …trials located in Lebanon, IN. This facility is Lilly's largest investment in a clinical trial manufacturing capacity and is intended to provide APIs for current ... making, drive progress, establish key performance indicators for work area and monitor effectiveness. + Forecasting resource needs across the integrated plan and… more
    Lilly (05/16/25)
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  • HVAC Engineer Lilly Medicine Foundry

    Lilly (Lebanon, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... plans, expense budgets, and prioritize appropriate Daily Support for operations: + Monitor utility systems and maintain KPI's to assure that they are operating… more
    Lilly (05/29/25)
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  • Electrical Engineer Power Distribution Lilly…

    Lilly (Lebanon, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... Training Requirements as the Equipment and Area SME Facility Operations: + Monitor , Assess and Document Equipment Performance to Maintain Ongoing Qualification. +… more
    Lilly (05/17/25)
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