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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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, 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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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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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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needed. Provide education and training to clinical staff on research protocols and procedures. Develop study-specific tools and manage biological specimen collection, processing, and shipping. Maintain
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and Senior QA Associate in achieving compliance with all Federal and State laws and regulations and other accrediting agency requirements in the collection, processing, preparation, and distribution
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. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
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. Additional responsibilities might be to oversee an MSAT team. As a successful candidate you will: · Oversee day to day activities related to facility and support as needed to ensure smooth operation of
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recruitment and pre-screening. Develop strategies for identifying potentially eligible patients for each study. Present trial concepts to research subjects and participate in the informed consent process
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, including logs for facility and equipment maintenance, autoclaves, RO systems, and cage wash operations. Research Support Assist investigators with setting up animal housing and procedure rooms, fogging