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program and its educational offerings. You will serve as a project manager, navigating the regulatory review process for each of their research studies, ushering manuscripts thru the submission and revision
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document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is
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of laboratory work area and furnishings/equipment · Receive, distribute and maintain supply inventories in laboratories as needed · Prepare simple stains, solutions, culture media, and process
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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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Hematology clinical trials. Familiar with Investigational New Drug procedures, study protocols, the informed consent process, Good Clinical Practices (GCPs), and applicable regulatory requirements. Required
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:00PM*** JOB SUMMARY Performs all tasks related to the admission/discharge/transfer process for all patient types. Performs accurate collection of patient demographic and insurance information, to be
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, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB protocol assuring that the documentation is complete and accurate in order to avoid
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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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/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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, Genomics, or a related field such as Computer Science, Biomedical Sciences, Molecular and Cellular Biology, or Cell Biology, with demonstrated computational expertise. Individuals with background in physical