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. To perform the informed consent process following GCP. To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance
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assessments such as adverse event (AE) information or questionnaires. Performs the informed consent process following GCP. The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer
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for advancement that other employers cannot match. DUTIES To conduct business requirements reviews, technical systems specifications and systems process analysis. To develop detailed selection evaluation criteria
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CLINICAL RESEARCH COORDINATOR I - (T227300) Description The University of Alabama at Birmingham (UAB), Surgery - Gen Surg Vascular Section, is seeking a Clinical Research Coordinator I. General
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process of assessing, planning, implementing and evaluating. To coordinate activities of other members of the interdisciplinary team to ensure quality patient care. Qualifications Associate's degree in
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for adherence to technical specification. Key Roles & Responsibilities · Perform modeling and simulation, processing and testing of materials, as well as collect, summarize, analyze and interpret data
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maintenance and development of the system. Best practices will guide departmental processes and system documentation to achieve an operational system that is supportable and maintainable. 6. Independently
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of procedures, protocols, information and techniques needed to diagnose and treat human injuries, disease and deformities · Knowledge and understanding of computer systems, tools and programs · Written and verbal
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optimal work flow and cost effective, quality patient care. Key Duties and Responsibilities : 1. Ensures smooth and efficient operation in area of responsibility. Maintains adequate staffing levels
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process, business, and technical requirement review. To partner with business experts to understand current challenges and collaboratively create solutions. To have a basic understanding of healthcare