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within the Department of Population Sciences and Department of Surgery with some guidance from a Ph.D. level Biostatistician. The incumbent will assist in the development of programs and databases using
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improvement processes and regulations for regions, across the enterprise and provide recommendations to study teams and clinical research leadership. Proactively engages in internal working groups, projects
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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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travel arrangements and preparation and processing of business expense reimbursement reports Assists with submission of program recertification and annual progress reports. Serves as intermediary
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pertinent clinical and protocol information on request forms. Develop and maintain knowledge of various aspects of processing specimens, with particular attention to safety practices. Identify and communicate
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purification, and co-crystallography studies that includes synchrotron data collection, and subsequent structural refinement, fragment-based drug discovery approaches, and computer aided drug discovery methods
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and corresponding protocol in order to determine coding and charge determinations. Enter and/or review financial data in OnCore and initiate the sign-off process of the OnCore calendar/financial console
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the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.
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with the QA Officer for preparedness for inspections by regulatory agencies so that there is a positive outcome and a minimum disruption in the daily operation and ensure that agency inspectors
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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