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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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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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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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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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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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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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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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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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The Office of Population Health Sciences (OPHS) at UIC is seeking applications for a Senior Clinical Research Coordinator II (Research Studies Manager). Certified Clinical Research Coordinator (CCRC), ACRP, SOCRA.
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We are seeking a motivated Research Associate/Senior Research Associate with broad experience and understanding of the small-molecule drug discovery processes. Deep understanding and hands-on experience with selected molecular techniques and cell-based assays, such as western blotting, DNA and RNA isolation, cell proliferation assays, cell cycle assays, apoptosis assays, MSD, incucyte, and flow cytometry.
$30 - $43 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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QualificationsEducational Requirements:High School Diploma/GED requiredBachelor's Degree in Science, Sociology or related degree preferredLicenses/Certifications:No license or certification requiredExperience:One (1) year of clinical research related experience preferredAbout UsCedars-Sinai is a leader in providing high-quality healthcare encompassing primary care, specialized medicine and research.
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Experience with analyzing electronic health records from multiple health systems, data visualization, geospatial programming, qualitative methods, creation of clinical decision support tools, implementation science and clinical and translational research.
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Texas Oncology is looking for a full-time Clinical Research Coordinator to join our team! What does the Clinical Research Coordinator do? Responsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject’s study visits and required activities per protocol.
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The Rehabilitation Aide (equivalent to the rehabilitation technician and physical therapy aide positions) will assist the Patient Experience Coordinator and clinicians by performing requested administrative and clinical duties.
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Prior experience conducting clinical research desired but not required; Under the supervision of Dr. Jeffrey Schnipper of the BWH Division of General Internal Medicine, the Clinical Research Assistant works directly with enrolled subjects as an essential research team member, tasked with the direct observation of in-hospital pharmacist workflow for a prospective pre-post mixed methods hybrid type 2 effectiveness-implementation study.
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clinical research patient experience jobs Title: research Company: Care Access
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