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submit data on appropriate forms according to protocol requirements. Ensure protocol compliance through intense monitoring of specific study requirements and schedule protocol-related activities. Play
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. As a successful candidate, you will: Responsible for overseeing the collection, documentation, and quality control of patient-reported outcome data. Collaborate with clinical PI, care team and patient
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regulatory requirements and the thorough collection, recording and maintenance of data and source documentation. The Clinical Study Coordinator collaborates with Investigators in review of subjects
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include not only operating the instrument but also assay development, sample preparation, calibration, data analysis, data management/backup and routine maintenance/trouble shooting. In addition, you will
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medicine, vascular biology, bioengineering, and data science, Dr. Chen leads an active research program focused on epigenetics, RNA and chromatin biology and endothelial stress response. Her team integrates
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. May modify protocols. Write standard operating procedures and reports. Maintain records of work performed, including results and methodology; utilizing records may calculate, graph, and compile data
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-paced research in cutting-edge technology, immunotherapeutic programs, and a commitment to delivering innovative solutions to critical illnesses. For more information on T Cell Therapeutics research
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current knowledge and requirements of relevant protocols. Performs extensive QC visits to confirm appropriate source documentation in electronic health record (laboratory data, transfusion services records
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improve the quality of life for our patients and their families. This position requires extensive experience in clinical and genomic data analysis techniques, as well as electronic medical record data
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with Principal Investigators (PIs) and their research staff including but not limited to clinical research coordinators, research nurses, monitors, data coordinators, as well as the various committee