• 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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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Indianapolis, IN)
    …/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols, GCP ... Tricuspid Therapies team. As the **Senior** ** Clinical Research Monitor ** , you ensure trial patients' safety by assuring trials are conducted ethically and… more
    Edwards Lifesciences (04/05/25)
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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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  • Senior Manager, Clinical Management

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …of assigned trial (s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity, trending and consistency.** ... of programs (eg, Word, Excel, PowerPoint, Outlook, etc.)** **Good understanding of clinical trial related software (eg, eCRFs, IRT, CTMS, etc.).** **Ability… more
    Otsuka America Pharmaceutical Inc. (05/13/25)
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  • Clinical Research Physician-Medical…

    Lilly (IN)
    …external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... and clinical data relevant to the molecule. Clinical Research/ Trial Execution and Support + Plans,...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
    Lilly (05/14/25)
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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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  • Senior Clinical Research Scientist

    Sumitomo Pharma (Indianapolis, IN)
    …Patient profile and data listing review experience. + Up to date in new clinical trial designs in oncology. + Strong analytical, problem-solving, and scientific ... clinical studies in close collaboration with the Clinical Research Team. + Monitor protocol compliance...collaboration with the Clinical Research Team. + Monitor protocol compliance including assessment of inclusion and exclusion… more
    Sumitomo Pharma (05/16/25)
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