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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Medical Center: UH: Clinical Lab (Full-Time, Night Shift) - Job Summary: The Clinical Lab Scientist 1, under general supervision, operates specialized instruments to conduct clinical lab tests and analyze data from results, to assist physicians with diagnosing medical conditions.
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MUST HAVE MS in Statistics/Biostatistics only with 1 year experience with statistical analysis, data wrangling, data cleaning, Power BI or Tableau, R programming, and SAS within a clinical setting.
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Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field of clinical research.
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The Clinical Data Coordinator must be able to review clinical trial protocols and understand inclusionary and exclusionary criteria for clinical trials. Review and abstract clinical data from electronic and paper medical records.
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The Clinical Research Coordinator II RN (CRC-II RN) serves the AdventHealth Research Institute (AHRI), under limited supervision, to plan, coordinate, evaluate and perform the nursing care of participants and collect data for assigned research projects.
$34.15 - $51.22Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Ensure high quality data collection activities by monitoring screening, enrollment and completeness of data collected on a weekly basis and report this information to the PI and clinical research coordinator.
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In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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The clinical research coordinator will be responsible for all aspects of study coordination including: subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up and regulatory documentation.
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As a Clinical Research Coordinator III, you will work independently providing study coordination including screening of potential research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Nola Hylton, PhD (Professor, Department of Radiology and Biomedical Imaging, Director, Breast Imaging Research Program, University of California, San Francisco) The Department of Radiology and Biomedical Imaging at UCSF is seeking a postdoctoral fellow interested in quantitative imaging and data science with application to breast cancer diagnosis and treatment.
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Central Research Support Staff: 7 (4 Grant Administrators, 1 Sr. Lab Manager, 1 Clinical Trials Manager, 1 Data Quality Director) Ensure that members of the DOS central research team, primarily grants administrators, meet regularly with individual PIs to review project timelines and benchmarks.
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Interpret requirements of functional areas and data analysts into consumable visualizations and analytics; apply multidisciplinary subject matter expertise in clinical nursing, medical devices, statistical analysis software, database management and data analytics.
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Performs nursing care, nursing assessment, and data collection for clinical research studies. The Simmons Cancer Center is seeking a Research Registered Nurse to join their Hematology and Oncology Disease Oriented Team. In this role, you will manage all patient activity on clinical oncology trials for the SCCC clinical trials at Parkland Hospital's Moody Outpatient Center Oncology.
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clinical research data review jobs Title: director biostatistics
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