• Associate - Trial Capabilities

    Lilly (Indianapolis, IN)
    …make life better for people around the world. Purpose: The Trial Capabilities Associate (TCA) provides clinical trial capabilities in support of ... maintenance and close-out. The TCA may be assigned responsibilities within any trial capability, including obtaining clinical trial authorizations and… more
    Lilly (08/22/25)
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  • Associate Director - Central…

    Lilly (IN)
    …other site staff. Lead internal relationships across the CDDA ( Trial Capabilities, Investigator Engagement, Patient Engagement, Clinical Design, Clinical ... make life better for people around the world. The Clinical Central Services and Innovation (CCSI) organization is responsible...but not limited to mobile health care, telemedicine, virtual trial orchestration, recruitment & retention, new site more
    Lilly (08/13/25)
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  • Associate Director - Clinical

    Lilly (Indianapolis, IN)
    …capabilities including but not limited to mobile health care, telemedicine, virtual trial orchestration, recruitment & retention, new site models, central ... to make life better for people around the world. **Purpose** The Clinical Central Services & Innovation (CCSI) organization is responsible for strategically planning… more
    Lilly (08/13/25)
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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...+ Review and set-up Protocol Specific Addendum (PSA) for clinical trials (the Associate will approve the… more
    Lilly (08/23/25)
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  • Associate Director - Site Systems…

    Lilly (Lebanon, IN)
    …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... on the Materials Flow Team, the role leads the site in optimizing our use of SAP technologies to...ensure the user and super user capability at the site for SAP and other core applications meets business… more
    Lilly (08/21/25)
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  • Oncology Regional Medical Scientific…

    Merck (Indianapolis, IN)
    …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... License:** Yes **Hazardous Material(s):** n/a **Required Skills:** Advisory Board Development, Clinical Engagement, Clinical Trial Support, Gastrointestinal… more
    Merck (08/23/25)
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  • Warehouse Associate

    Bristol Myers Squibb (Indianapolis, IN)
    …role, the Warehouse Associate shall provide tactile support of all clinical trial and future commercial receiving, material handling, shipping and ... for warehousing support related to domestic and international shipping and distribution of clinical trial and commercial products for RayzeBio programs. In this… more
    Bristol Myers Squibb (08/24/25)
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  • Associate Director, Small Molecule Process…

    Lilly (Lebanon, IN)
    …resilience as the site evolves from a design concept to a GMP clinical trial site . **Key Responsibilities:** + Responsible for establishing a technically ... develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental… more
    Lilly (08/19/25)
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  • Sr. Director, ExploR&D Clinical Operations

    Lilly (IN)
    …and effectively utilize for delivering the portfolio. + Collaborate with Clinical Operation Associate Director/Director to stimulate, collate, and facilitate ... The purpose of the job is to ensure ExploR&D has adequate Good Clinical Practices (GCP) systems in place that are properly executed. Responsibilities include… more
    Lilly (08/17/25)
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  • Associate Medical Director,…

    Sumitomo Pharma (Indianapolis, IN)
    …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director.** The Associate Medical Director...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… more
    Sumitomo Pharma (08/15/25)
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