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Clinical Research Coordinator B: Bachelor's degree and 2-3 years of experience, or equivalent combination of education and experience, are required. Clinical Research Coordinator C: Bachelor's degree and 4-5 years of experience, or equivalent combination of education and experience, are required.
$43,919 - $67,046 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Minimum three years of experience managing and supervising a research team or five years leadership experience in the clinical research capacity. Posted job title: Manager, Clinical Research (Rn) About Saint Francis Health System Saint Francis Health System is a Catholic, not-for-profit health system wholly owned and operated in Tulsa, Oklahoma whose mission is to extend the presence and healing ministry of Christ to all who seek its services.
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Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it.
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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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The research portfolio of the Dermatology Service includes optical engineering, artificial intelligence, basic science, translational science, epidemiology and clinical trials with over $5 million of annual funding from NIH, Foundations, Industry, and philanthropic sources.
$150,000 - $510,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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He or she will perform a preliminary protocol assessment with the Supply Chain Lead (SCL), Clinical Research Pharmacist (CRP) and clinical team members (e.g., clinician, biostatistician) to determine the most effective IRT strategy for clinical customer, investigator site, Global Clinical Supply, and ultimately for the patient.
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Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service.
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Keywords : clinical research, CRC, clinical research coordinator, clinical trials, orientation, training, informed consent, central lab management, data management, expectancy reports, visit preparation, low institutional risk trials, IRB submission, IRB approval, GCP, good clinical practice, train, supervise, institutional review board, regulatory, grants, quality control, QC, clinical trial data, EDC, patient data, admin, administrator.
$50,000 - $65,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with clinical sample handling and inventory management is strongly preferred. Experience using multi-color panels for flow cytometry. Perform complex multi-color flow cytometric analysis of manufactured product and clinical samples to evaluate key biomarker expression.
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The Clinical Research Coordinator (CRC) will oversee the execution of research studies according to established study protocols. The CRC will have direct contact with research participants, manage multiple clinical research projects/trials, and serve as a backup to other clinical research coordinators within the team.
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Hands-on laboratory research experience in biochemistry/cell/molecular biology, immuno-oncology, or related disciplines (and corresponding instrumentation. Collaborate with translational research teams to develop and implement sample management system for appropriate handling, storage, and documentation of preclinical and clinical samples.
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Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials. A thorough understanding of regulatory policies governing industry practices, HIPAA requirements for clinical research, and knowledgeable about patient safety and quality control requirements.
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The mission of the UCSF HDFCCC clinical research program is to provide patients and their families with streamlined access to cutting-edge cancer therapies, In addition to providing compassionate, patient-centered care, our team of clinicians and researchers is dedicated to improving outcomes for all patients.
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We welcome applicants reflecting the broad diversity and lived experiences in our communities Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials.
$36,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A successful applicant should have a background in biomedical research, engineering, neuroscience, biomechanics, or a related discipline with knowledge or interest in physiology, rehabilitation, and biomedical/clinical principles.
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clinical research patient experience jobs Title: research assistant Company: Care Access
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