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candidate you will: · Shepherd protocols through the C/PRMC and IRB review processes to achieve a timely outcome that is compliant with applicable regulations. · Manage new protocols
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, protocols, amendments, correspondence and serious adverse event reports. Performs extensive audits and monitoring visits to determine protocol compliance, including the consent process and eligibility
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, RT-PCR, and cytotoxicity assays, under minimal supervision. You will provide supervision and training to junior team members and support the qualification and validation of manufacturing processes and
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the System Clinical Research in the development of best practices and tools for protocol execution, management and oversight in the feasibility and startup process. The Director ensures strong communication
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concepts and details to the research subjects, participates in the informed consent process, enrolls, and coordinates care of subjects in compliance with protocol requirements. The CSC may provide education
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research-related documents. You will serve as a project manager, navigating the regulatory review process for each research study, ushering manuscripts through the submission and revision process, and
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tissue collection), DNA extraction, PCR analysis, histological techniques, fluorescent microscopy, computer skills (word processing, email, spreadsheet management, adobe photoshop, Image J), and lab
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, ligation, suture), vascular/endothelial biology, RNA/chromatin biology, immunohistochemistry, immunology, sequencing analysis and bioinformatics, flow cytometry and imaging-based analyses, tissue processing
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strategy for identifying potentially eligible patients for each study. The CRN presents trial concepts and details to the research subjects, participates in the informed consent process, enrolls, and
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Medicine, and member of the City of Hope Comprehensive Cancer. The Perry laboratory uses structural biology approaches, together with small molecule and fragment-based drug discovery, computer-aided drug