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candidate, you will: · You must have experience with flow cytometry, molecular biology techniques, cell culture, microscopy, tissue processing, immunohistochemistry, immunofluorescence, data analysis
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including study documents, research calendars, data collection tools, and its comprehensive financial system in an efficient and timely manner. This role will report to the City of Hope Director of Clinical
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protocols, while maintaining high standards of scientific rigor. Accurately record, analyze, and validate experimental data; generate figures and summaries to support ongoing projects and publications
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; and managing inventory and supply lists.Additional duties include assisting with specimen or data collection for research projects or demonstrations; cleaning and maintaining glassware and laboratory
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protocols to ensure efficiency and regulatory compliance while attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an effective system for data flow
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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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current and accurate protocol documentation; notify investigators of pertinent protocol changes. Maintain and complete regulatory documents for IRB, DSMB, and PRMC/CPRMC. Compile and submit data
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store blood samples following study and safety guidelines. Utilize EPIC and various sponsor web portals for study documentation and data entry. Perform other duties as assigned to support research
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successful candidate, you will: · Design and perform experiments and analyze data · Regularly communicate and interact with the other team members · Submit abstracts to scientific
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corresponding data into the institution’s OnCore Clinical Trials Management System (CTMS). Critical to this work is the development of a clinical trial’s calendar within the CTMS that forms the backbone