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Regulatory Coordinator at City of Hope, you'll play a crucial role in assisting our investigators with the submission of human subject research to regulatory committees, contributing to the advancement
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activation of human subject research to regulatory committees. This includes facilitating prompt submission of protocols, amendments, and updates to regulatory oversight committees and acting as the primary
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oncology therapies while working in a fast-paced environment. Trial responsibility ranges from First in Human and Phase I-Phase III clinical trials, in addition to Investigator Initiated Trials( IIT’s
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-doctoral fellowships), involvement with human observational or therapeutic studies, protocol design/writing for human sample, observational/retrospective or therapeutic studies. Familiarity with data
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ranging from underserved human communities to naturally occurring canine and chicken cancers. This position requires the employee to be a lab leader and perform all duties related to experimental design and
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underserved human communities to naturally occurring canine and chicken cancers. Under management supervision, this position requires the employee to perform all duties related to experimental execution, basic
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, infectious hazards, radioactive materials, and radiation producing machines. Familiarity with federal and California regulations on human subjects research. City of Hope is an equal opportunity employer
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3 years of employment • International Air Transport Association (IATA) within 1 month of employment • Good Clinical Practice (GCP) within 1 month of employment • Human Subjects Protection (HSP) within
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will: Ability to carry out cell culture experiments using transfection agents and RNA isolation to perform RT PCR experiments. Willingness to learn animal handling and testing with humanized mouse models
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in clinical research protocols through clinician interactions and medical record reviews. As a successful candidate, you will: Conduct laboratory tasks: preparing sterile solutions, processing human