• Associate Director - Clinical Development,…

    Lilly (Boston, MA)
    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 (07/31/25)
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  • Post-Approval Compliance Monitor

    Alaka'ina Foundation Family of Companies (Silver Spring, MD)
    …best practices REQUIRED SKILLS AND EXPERIENCE: + Minimum three (3) years experience as a Clinical Trial Monitor + Knowledge and experience in the areas of ... Post-Approval Compliance Monitor Location MD - Silver Spring Job Code 13020 # of openings 1 Apply Now… more
    Alaka'ina Foundation Family of Companies (06/21/25)
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  • RN Clinical Research Coordinator

    Novant Health (Winston Salem, NC)
    …routine clinical trial related activities. Collects, enters and summarizes clinical trial data. Monitor patients, their results, detects and reports ... study investigators. Clinical Research Coordinators facilitate and coordinate daily clinical trial activities and play a critical role in the conduct of the… more
    Novant Health (07/30/25)
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  • Associate Director, Digital Clinical

    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. Specifically: + Identify and define Clinical more
    BeOne Medicines (06/07/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Seattle, WA)
    …/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 (07/31/25)
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  • Clinical Trials Monitor - Pediatrics

    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 (07/23/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Helena, MT)
    …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 Trial Support Coord

    Premier Health (Centerville, OH)
    …in development of monitor plans. Other duties may include reviewing clinical trial data, including trending statistics, developing case report forms (CRF) ... Facility: Miami Valley Hospital South Position Summary General Summary/Responsibilities: The Clinical Trial Support Coordinator will function in a multi-faceted… more
    Premier Health (07/25/25)
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  • Senior Clinical Trial Operations…

    HonorHealth (AZ)
    …of the study. The position's competencies include project management, clinical trial operations, coding/billing compliance, Medicare coverage analysis/budgeting, ... contracting, Clinical Trial Management Systems (CTMS), and basic finance and accounting...supplies, departmental, contractors/vendors). Partner with Research Program Managers to monitor resources to ensure that they are properly allocated… more
    HonorHealth (07/23/25)
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  • Clinical Trial Specialist

    Caris Life Sciences (Phoenix, AZ)
    …bigger than yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist provides operational and regulatory support for the ... Initiation Visit meeting and offer ongoing site support. + Monitor and facilitate local site IRB and central IRB...have 1-2 years' experience in a Biorepository setting or Clinical Trial setting. + Experience in handling… more
    Caris Life Sciences (07/09/25)
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