83 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"Dr" positions at City of Hope
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attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an effective system for data flow. Benefit from mentorship by experienced staff in a dynamic research
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extensive review of case report forms and study data, utilizing medical records, laboratory data, transfusion services records, and any other source used to produce study data. Generates an audit report or
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computational methods for cancer pangenomics using long-read sequencing data. Through TGen's Collaborative Sequencing Center (CSC), we have access to in-house PacBio Revio and Oxford Nanopore PromethION platforms
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involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory
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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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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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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