622 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" positions at University of Alabama at Birmingham
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, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program
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improvements or technology integrations, to enhance operational efficiency in clinical settings. Analyze data and compile comprehensive reports on budgets, personnel, space utilization, and clinical performance
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data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork. Key Duties & Responsibilities Responsible for completing Case Report
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evaluate patient’s medical record and social data. To perform and/or assist the physician with procedures per collaborative agreement. To coordinate and participate in performance improvement activities. Key
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retention efforts, data quality control, and regulatory compliance. General Responsibilities To serve as coordinator for studies and provide support to other team members within the confines of the protocol
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, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork. Key Duties & Responsibilities Conducts
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and manage clinic calendars Complete patient registration and verify demographic, insurance, and appointment information Accurately enter and update patient information in electronic medical record (EMR
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Research Interviewer - Temporary - (T231272) Description The Research Interviewer is responsible for collecting patient and participant information in accordance with established research protocols
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Affairs HR service team, this position provides comprehensive support for projects, reporting, and data management across all personnel processes. The role ensures full compliance with licensure
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assessments such as adverse event (AE) information or questionnaires. To perform the informed consent process following GCP. To act as a liaison between the clinical and research staff, departments, ancillary