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Conduct patient recruitment and scheduling, data collection and management, specimen collection, handling and processing, compliance with IRB regulations and communicating with team members on the status of projects.
$16.42 - $22.57Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Instructs employees and students in phlebotomy, data entry and specimen processing functions. Ensures completion of specimen collection functions according to protocol.
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Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
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Provides leadership to the research team in ensuring collection of source data and completion of documentation that validated the integrity of the research. Demonstrates leadership in ensuring adherence to ethical practices during the conduct of research to protect the rights and well-being of patients and the collection of quality data.
$31.34 - $48.82 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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A Clinical Research Coordinator (CRC) is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
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Coordinate assigned protocols, including patient enrollment, data abstraction, case report form completion and submission, specimen shipping, and other protocol-related tasks. Under the supervision of Principal Investigator and Research faculty, we are seeking a Research Program Coordinator who will be responsible for administrative, regulatory, operations support, and data collection/maintenance for ongoing clinical research studies.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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A Research Coordinator is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs and GCPs.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Performs Venipuncture and collects other specimens from newborn, pediatric, and adult patients according to established protocol. Responds to additional specimen procurement requests via pager or other means.
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Processes specimens for testing, including aliquoting, pre-analytical steps, and loading instruments, while maintaining proper specimen identification. Documents appropriate information for quality assurance/improvement according to established protocol.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
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