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Develops highly complex clinical trial budgets sponsored for industry and the National Institutes of Health (NIH), investigator-initiated clinical research. The Clinical Research Budget Coordinator III develops highly complex clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research.
$64.02 an hourFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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3 + years of experience in clinical research and/or bioethics with preferred experience directly related to safety & pharmacovigilance. Maintain document control for safety & pharmacovigilance electronic files, perform file case searches & queries, maintain trial databases and ensure all files are up to date and accurate.
$150,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Whether you are healthy, or have a specific illness, we'll connect you with the right trial. Potentially get paid to access the most cutting edge medicines combating your disease. Whether you are healthy, or have a specific illness, we'll connect you with the right trial.
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Most trials don't require much effort and will be located near you.
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Most trials don't require much effort and will be located near you.
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Under the guidance of the Clinical Trial Manager, the Clinical Research Coordinator (CRC) III functions independently and proficiently with minimal oversight and is responsible for the complete coordination of assigned clinical research activities of all phases and all levels of complexity, including investigator-initiated or other high profile research.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations; Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The CRA works closely with the Clinical Trial Manager (CTM) and/or lead CRA to ensure all monitoring activities are conducted according to study requirements and Monitoring Plan. The CRA may report to a CTM or people manager and has no direct reports.
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Utlize OnCore CTMS, Cerner Revenue Cycle and Power Trials to support an efficient clinical trial revenue cycle process. Ensure timely and accurate clinical trial invoicing as assigned.
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We are seeking a Clinical Trial Assistant with 1-2 years of Clinical Research Coordinator experience. Job Title: Clinical Trial Assistant. We are seeking a Clinical Trial Assistant with 1-2 years of Clinical Research Coordinator experience.
Part-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Ability to analyze clinical research protocols, assess study budgets, and analyze clinical trial contracts including payment terms. Acts as a resource in the development of internal policies, procedures and job aides related to clinical trial billing.
$105,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Maintain a current clinical trial and clinical research study Good Clinical Practice GCP knowledge base, in order to serve as an expert resource to the client in a regularly changing field, and addresses identified knowledge and skill gaps related to role.
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Job OverviewThe Clinical Research Nurse Coordinator 1 serves as coordinator for phase I, II and III oncology clinical trials conducted in the Center for Translational Transplant Medicine, in duties that include but are not limited to:Provides overall coordination of assigned clinical trials throughout the trial lifecycle.
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The Senior Applications Administrator, Clinical Research Programs functions as the Subject Matter Expert for Clinical Research computer applications at for the GW SMHS and reports within the Office of the Dean. This includes the Clinical Trial Management System ( CTMS )-Oncore™, Eval, Oncore™- Electronic Data Capture ( EDC ), Florence eBinders (eRegulatory system and econsenting module) and other systems.
$109,234.47 a yearFull-timeExpandApply NowActive JobUpdated Today
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