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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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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
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of new and improved techniques. Ensure that all laboratory activities are carried out in compliance with each procedure(s) by utilizing safety procedures and guidelines in handling, storage and disposal
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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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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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. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.