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to support in-process and release testing for GMP Manufacturing and gene and cellular immunotherapy products. This fast-paced lab uses cutting-edge technology for clinical immunotherapeutic programs, including
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research in partnership with Department Surgery clinical and research faculty members. This will be a joint appointment in both the Department of Surgery and Division of Biostatistics at a rank and salary
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/transfer process for all patient types. Performs accurate collection of patient demographic and insurance information, to be verified upon each patient registration. Performs check-in, check-out process
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for the general review and processing of invoices comprised of charges for the Shared Resources for BRI. Performs review of charges for usage of shared resource billing system for accuracy. Prepares invoices
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protocol deviations. Manage patient/family phone calls – collaborating with MD, NP and/or PA as needed to obtain orders for the management of the patient. Ensure the consent process is performed in
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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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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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, 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