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other databases. Ensures regulatory documents are properly completed and filed, serves as a liaison between investigators, IRB, REDCap, and other relevant healthcare professionals who are part of
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with UIC information technology research infrastructures, e.g. REDCap, UIC Advanced Cyberinfrastructure for Education and Research (ACER), Azure SCE, UIC IRB and UI Health data regulations and policies
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including Institutional Review Board (IRB) & federal or industry sponsor processes and requirements; ACRP (Assn of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates
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. This position will be responsible for completing case report forms (CRFs), entering clinical research data, and assisting with regulatory submissions to the Institutional Review Board (IRB). The CRA I member may
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implementation status and make recommendations on operational issues. Assist with the preparation of submissions to the Institutional Review Board (IRB). Liaison with IRB on administrative matters and facilitate
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updates on protocol implementation status and make recommendations on operational issues. Assist with the preparation of submissions to the Institutional Review Board (IRB). Liaison with IRB
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to all University guidelines and good clinical practices. Collect samples/phlebotomy. Prepare and maintain regulatory documentation, including IRB initial submissions, modifications, and continuing reviews
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or recent liver transplant. The coordinator’s responsibilities will include maintaining and updating IRB protocols, patient identification through an electronic health record, patient recruitment, ensuring
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. Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC. Assists faculty in the preparation of grant submissions and associated documentation
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. Assists in the preparation of materials, submissions and renewals to the Institutional Review Board (IRB) or IACUC. Assists faculty in the preparation of grant submissions and associated documentation