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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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Collaborate with cross-functional teams, including Clinical Management, Clinical Development, Pharmacovigilance, Biostatistics, Data Management, Medical Writing, Asset Management and IT, to ensure agreement on analysis and reporting deliverables for clinical trials and projects.
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DCAC is an in-house centralized resource for clinical data management, biostatistical analysis, reporting, and training in support of clinical trials and scientific research.
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Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance) for monitoring and site management activities.
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Similar searchable job titles Clinical Quality Manager Health Information Management Supervisor Quality Improvement Coordinator Clinical Data Quality Analyst Healthcare Compliance Officer Keywords Health Information Management Clinical Quality Reporting Data Migration Regulatory Compliance Quality Improvement Legal Disclaimer: Cherokee Federal is an equal opportunity employer.
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The Director must understand the entire preclinical and early clinical product development pipeline including product optimization, preclinical scale-up, and manufacture and toxicology, regulatory affairs, and early human clinical trials.
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Peraton's DSCM program encompasses technical, engineering, data analytics, cyber security, management, operational, logistical and administrative support to aid and advise DoS Cyber & Technology Security (CTS) Directorate.
$86,000 - $138,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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As R Shiny programmer you will design, develop, deploy, and optimize user-friendly interactive web applications for clinical data analysis and visualization. We are seeking a talented R Shiny programmer to facilitate interactive reports that translate clinical trial data into clinical insights.
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Senior director, clinical program lead, late-stage clinical development, clinical trials, global, strategy, hematology, lymphoma, oncology, targeted therapies, ADCs, antibody-drug conjugates, program, asset, label extension, life-cycle management, pharma, biotech, biopharma, MD, medical doctor, phase I, phase II, phase III, FDA.
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Maintain and manage all products in the IRS portfolio, including PowerCenter, PowerExchange, Data Quality, Data Transformation, Test Data Management, Change Data Capture (CDC), Enterprise Data Catalog (EDC), Axon, and Intelligent Data Management Cloud (IDMC)/Informatica Intelligent.
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Interact with clinical scientists, data management, statistical programming, data standard team to streamline data quality review process for real-time data quality monitoring.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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We're looking for our next Data Operations Analyst who has a particular specialty or interest in web scraping and extracting data from the open source. Experience, education or interest in business intelligence research, conflict and illicit finance analysis, banking sector risk management and compliance or national security-related matters will catapult your success in this role as these elements are core to our business.
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Under the guidance of the mentor, the participant will gain a greater understanding and working knowledge in the design and conduct of clinical trials and expertise in the use and considerations of biomarkers and surrogate endpoints in rare disease drug development.
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clinical trials data management jobs Title: operations in Bethesda, MD
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