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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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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.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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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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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 1 month ago - UpvoteDownvoteShare Job
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Job Summary: The Research Assistant supports patient assessment and data entry activities for research studies. Performs data entry activities; records essential data onto the required study forms and reports, submitting them in a timely manner.
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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.
$21.55 - $35.57 an hourFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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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.
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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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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.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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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 10 days 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.
Part-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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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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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.
$25.96 - $31.25 an hourFull-timeExpandApply NowActive JobUpdated Yesterday
data entry jobs Title: assistant clinical research in Phenix-city, Alabama
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