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Provides clinical support to products entering or currently on the market including training BD associates, troubleshooting, data review, interpretation and presentation, post market study design, publications, preparation or review of regulatory communications, and addressing quality issues.
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Review, analyze, and interpret emerging clinical trial data (including biomarkers, clinical pharmacology, and safety data) and lead preparation for key study meetings (e.g. investigator meetings, monitoring committees, advisory boards.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Assume medical responsibility for clinical trials including active participation in real-time medical monitoring of studies, including patient eligibility assessment, study design questions, accrual, and safety data review.
Full-timeRemoteExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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You’ll work on materials developed from statistical data, medical information, clinical studies, and market research, while adapting to unique brand guidelines and editorial style guides.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Expertly mine, review, dissect and interpret clinical trial business intelligence information, data analytics, site reported data and systems in various formats to apply to individual assessments, drive multi-functional discussion and derive recommendations related to protocol, country, accrual rate and site components of assigned assessments.
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Ability to design and conduct clinical research activities and perform data analysis. Knowledge of and experience in Quality Assessment and Improvement, Utilization Review.
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Oversees the planning and performance of compliance audits of foreign and domestic clinical investigators to verify protection of human research participants, data integrity, and regulatory and protocol compliance.
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The incumbent assesses the request, conducts all necessary research such as verifying benefit coverage for the patient, and then creates the case (data entry) in Highmark's utilization management system for clinical review.
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2+ years of hospital / reference clinical laboratory or related healthcare field experience, or clinical research. · Provides medical expertise and leadership for Human Factor Engineering (HFE) studies, Health Economics & Outcomes Research (HEOR) studies, post-market surveillance and post-market studies.
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This is a high travelling, on-site monitoring contract Clinical Research Associate opportunity for a West-Coast based Contractor. 10+ years of experience as a Clinical Research Associate.
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Reviews and queries safety and efficacy data in support of the clinical data review strategy and collection of quality data and review of emerging clinical data and trends; presents and discusses relevant data to appropriate teams, governance bodies, and other internal and external stakeholders.
$218,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Executes HEOR research using internal data sets including writing protocols and statistical analysis plans, defending in protocol review committee, and executing research with analyst to writing final reports or publications using prospective, retrospective, modeling, PRO's, meta analyses and hybrid designs.
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The Data Engineer/Software Developer participates in full life cycle application development; designs and support complex scientific software development and deployment for basic and clinical research studies.
$135,285 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform clinical data reviews, identify data trends, and assess protocol deviations; ensuring resolution of identified issues during data review and protocol deviation reviews cross‐functionally and with sites in collaboration with the study team.
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We are seeking a highly skilled Sub-Investigator (Nurse Practitioner) to support clinical studies in Washington Heights, New York City, NY. The successful candidate will play a crucial role in the execution of these industry-sponsored trials, ensuring adherence to study protocols and contributing to the advancement of vaccine research.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical research data review jobs in Hoboken, NJ
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