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Interpret patient clinical information from electronic medical records (EMRs) for participation qualification and data entry. Complete all clerical data entry associated with each case or as assigned.
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1-3 years of research experience, including data entry, and data management. Support clinical research reporting for data review, quality control checks, and interim and final analysis.
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10% - The Program Assistant will perform simple data entry to study databases in a timely manner. The Clinical Research Assistant is responsible for coordination of investigator-initiated transplant studies for the Department of Surgery as directed by the Principal Investigator.
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Assist in coordinating the details of the study and documentation concerning study protocols, patient scheduling, history work, data collection, data entry, data management, follow-up care, and compliance with federal, state, sponsor and institutional guidelines.
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Complete data entry and verification into required databases, including RAVE and REDCap. Demonstrated experience with performing data entry into registry or database. Minimum one year of experience in clinical trial protocol management, including but not limited to preparation of regulatory submissions, recruitment of eligible patients, and reporting of study data.
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The CRA be responsible for data entry, coding and quality checking. Temporary Clinical Research Assistant. Penn's Laboratory for Cognition and Neural Stimulation (LCNS) in the Department of Neurology has a 10-20 hour per week position available in clinical research.
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The Research Assistant will be responsible for data entry, laboratory procedures such as blood draws, and other administrative tasks as required. Clinical Research Professionals is looking for a Clinical Research Assistant to assist coordinators in conducting clinical research study visits.
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Apply clinical knowledge and skills that will assist the Clinical Research team in data entry and maintenance of patient care records as it relates to Clinical Trials for Oncology patients.
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Job DescriptionJob DescriptionJob descriptionPOSITION SUMMARY:The position of Clinical Research Assistant assists research department with the conduct of new and active research studies, including but not limited to data management, patient scheduling, filing, obtaining research team member signatures, patient screening, and follow-up, transporting study materials (including biological specimens), obtaining patient informed consent, and creating and maintaining study documentation.
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The Clinical Research Assistant assists in entry level clinical research activities and plays a vital role in supporting clinical research activities within The University of Kansas Cancer Center.
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The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.
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The CRC-A is the entry position in the Clinical Research Coordinator series. Duties include but are not limited to study recruitment, data entry, maintenance of study records, management of study materials, and specimen processing, storage, and shipment.
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This position coordinates aspects of the clinical studies including providing pivotal response treatment to young children with autism at in-home sessions, in the outpatient Child Psychiatry Division at Stanford and/or at a Stanford satellite classroom in San Jose. The position also requires assuring accurate data collection and entry and assisting with participant recruitment for research studies.
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Assist Project Manager in tracking participant and study progress, monitoring active participants, record-keeping, data entry and verification, filing, collection and processing of biological materials (e.g., saliva, blood, urine, feces), and other assigned duties.
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Conduct ongoing audit and quality control of structural and functional data collected by site investigators in the ongoing NIH-funded COAST trial (involves ensuring timely performance of required testing, assessing quality metrics, ensuring concordance between test results and data entry, timely retesting as indicated, etc.
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data entry jobs Title: assistant clinical research in Phenix-city, Alabama
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