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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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Completes data entry into case report forms ensuring accuracy of data and reporting of adverse events to sponsor; Ensures study related reports and patient results are reviewed by the Clinical Research Coordinator and/or Investigator in a timely manner; Organizes work area.
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As part of the Pulmonary Ambulatory Clinical Trials (PACT) group, the coordinator will perform study procedures per the research study protocols and regulatory requirements, including participant recruitment, data and specimen collection, study procedures, data entry and organization of study records, adverse event reporting, and study invoicing.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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The CRA I will offer a spectrum of study-related services, including participant recruitment, consenting, coordination, query resolution, database creation, completion of source documents and case report forms, as well as data entry.
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May coordinate activities and participate in the training of volunteers or others assigned to research projects to interview participants to complete forms or to perform data abstraction or data entry duties.
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Help study coordinator maintain research charts and binders and do data entry including extracting data from medical charts. In addition to above, will be expected to do more in-depth prescreening and review of medical records, data entry, and conduct study visits and procedures autonomously.
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Responsibilities: Review medical records and assist with data extraction, entry, and submission Assist with participant recruitment, screening, scheduling and conducting visits Assist with data quality control Assist with scheduling and conducting monitoring visits and query resolution Request medical records and images Assist with bio-specimen processing and tissue requests Schedule patients for research appointments Perform other duties as assigned by project leader or management.
$20 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure study preservation through scheduling and coordinating study visits, managing EDC data entry and queries, and follow-up of patients within the study. As an assistant, you will work on a research team composed of clinical research coordinators, while also working hand-in-hand with orthopedic surgeons, fellows, medical students, physical therapists, amongst other providers at the Steadman Hawkins Clinic of the Carolinas in Greenville, SC.
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If you are a Clinical Research Assistant or Coordinator looking to get into Data and Quality, please consider applying as well. The Quality Control Data Management Specialist entails quality control and precise data entry for clinical studies, under the supervision of the Operations Manager.
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Entry-level position responsible for assisting the Clinical Research Associate in conducting Phase I - IV clinical studies according to ICH guidelines. Experience working with biological specimens and data sets, ideally with some clinical trial familiarity Will be providing general administrative support to the Medical, Clinical, and Scientific Organizations and assistance to department Manager(s) and Director(s.
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Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities.
$26.29 - $42.28 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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This is a part-time hybrid role as a Clinical Research Assistant at NEERA. The Clinical Research Assistant will be involved in various day-to-day tasks including data collection and entry, participant recruitment, and documentation.
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This is an excellent opportunity for clinical research professionals to get into data and quality! Additionally, the role involves collaboration with clinical research teams and sponsor representatives, attending meetings, assisting in sponsor visits, and supporting training procedures, with a focus on professionalism and efficiency.
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