144 information-security-"https:"-"https:"-"https:"-"https:"-"https:" positions at City of Hope
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multi-site research. · Oversee data management systems for secure archiving, traceability, metadata capture, and reproducible quantitative analyses. · Manage scheduling, staffing
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evaluates data and suggests alternative approaches for improvement. · Trains lab staff in specialized procedures, equipment, and theoretical concepts. · Ensures compliance with safety procedures
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, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management
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eligibility, safety, and protocol adherence, and report adverse events promptly. Pursue continuous education and training opportunities, staying updated with the latest clinical research information, and
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; utilizing records may calculate, graph, and compile data. Develop techniques and expertise in one or more areas relevant to laboratory research projects. Ensure that all laboratory activities are carried out
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Research Execution Establish and maintain systemwide standards for trial execution, patient safety, protocol compliance, and accurate data collection. Ensure strong relationships across clinical research
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-edge research. A Research Associate II opportunity is immediately available for a highly motivated individual in the laboratory of Ling Li, Ph.D., in the Department of Hematological Malignancies
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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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Thank you for your interest. Please note, the purpose of this posting is to recruit for on-going and future positions. Join the forefront of groundbreaking research at City of Hope where we're
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, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management