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-process and release testing of GMP Manufacturing and analytical development for cellular immunotherapy products. This is a fast-paced lab involved in cutting edge technology, research and clinical cellular
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to the research subjects, participates in the informed consent process, enrolls, and coordinates care of subjects in compliance with protocol requirements. The CRN may provide teaching on investigational agents
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, shaping the future of medicine through cutting-edge research. The QC team for Cellular and Gene Therapy Operations seeks a skilled Quality Control Manager to oversee in-process and release testing for GMP
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, Journal of Immunology , Journal for Immunotherapy of Cancer , International Journal of Radiation Oncology* Biology* and Physics , and other journals. City of Hope is an equal opportunity employer. To learn
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. The successful candidate: Hours: Part time, Thursdays only (12hrs per week) Performs all tasks related to the EHR admission/discharge process of outpatient and inpatient visits. Performs accurate patient
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data reporting requirements. Review and process invoices from sub-sites. Regulatory Responsibilities for Participating Sites: Manage deviation, adverse event, and unanticipated problem reporting. Systems
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in to IRB clinical trials. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB
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revising Standard Operating Procedures as necessary for cell product manufacturing and process development. · Cooperate with Quality Control (QC) and Quality Assurance (QA) groups to ensure
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consent documents · Coordinate responses during the protocol approval process, interfacing with internal stakeholders Your qualifications should include: · Master's degree or Bachelor's degree
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: Prepare media and buffers, conduct islet cell count and viability assays, and conduct functional tests including but not limited to ELISA. Culture islet cells for QC assays and process clinical research