• 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 Manager, Digital Clinical Operations…

    BeOne Medicines (San Mateo, CA)
    … Operations' productivity, reduce rising costs of clinical trials, and reduce clinical trial inefficiencies + Monitor , evaluate, and optimize the ... with the goal to increase Global Clinical Operations' productivity and reduce clinical trial inefficiencies. This will be achieved by: + Supporting the… more
    BeOne Medicines (03/08/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (San Francisco, CA)
    clinical trial /study subject documentation aligns with the study hypothesis and monitor clinical trial /study safety in accordance with protocols, Good ... Field Monitoring team. As the Senior Clinical Research Monitor , you will ensure trial patients' safety by assuring trials are conducted ethically and within… more
    Edwards Lifesciences (04/23/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Des Moines, IA)
    …/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols, GCP ... Monitor ** to join Edwards Aortic Field Monitoring team. As a Senior Clinical Research Monitor , you ensure trial patients' safety by assuring trials are… more
    Edwards Lifesciences (04/22/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Pittsburgh, PA)
    …/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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  • Clinical Trials Monitor - Breast…

    Dana-Farber Cancer Institute (Brookline, MA)
    …by utilizing monitoring tracking forms and other monitoring related tools and templates. + Monitor clinical trial progress through a combination of remote ... The Clinical Trials Monitor helps to ensure...reports. + Assist in the development and writing of clinical trial monitoring plans. + Provide recommendations… more
    Dana-Farber Cancer Institute (05/08/25)
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  • Manager, Clinical Supply Chain

    BeOne Medicines (San Mateo, CA)
    …and timelines. + Create supply and inventory plans and develop production schedules for clinical trial materials. + Monitor schedule adherence of production ... **General Description:** The Manager of Clinical Supply Chain manages drug supply activities related...label & pack, and distribution for one or more clinical programs. Actively develops and oversees supply plans to… more
    BeOne Medicines (04/05/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Providence, RI)
    …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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  • Clinical Operations Manager

    Edwards Lifesciences (Irvine, CA)
    trial documentation is within parameters of study protocol, as well as to monitor clinical trial /study safety, in keeping with protocols, GCP (Good ... a team of in-house clinical research professionals, overseeing all clinical trial related Clinical Imaging and Core Lab management activities. Establish… more
    Edwards Lifesciences (04/19/25)
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  • Clinical Research Associate

    Hartford HealthCare (Hartford, CT)
    …associated with meeting the goals outlined in the protocol and clinical trial agreement * Motivate others, monitor study performance and lead study meetings ... for the overall design, conduct, and management of the clinical trial , the CRA leads, facilitates and...* Set-up of new studies into the CTMS * Monitor the CTMS system for accuracy of data *… more
    Hartford HealthCare (04/15/25)
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