At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advance health together. What You Can Expect Pursue your passion for caring with Duke University Hospital in Durham, North Carolina, which is consistently ranked among the best in the United States. The largest of the four Duke Health hospitals with 1062 patient beds, it features comprehensive diagnostic and therapeutic facilities, including a regional emergency/trauma center, an endo-surgery center, and more. How You Will Make An Impact The Clinical Research Coordinatoe will coordinate and participate in clinical research studies conducted by principal investigators at Duke University Medical Center. Coordinate and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Coordinate and perform study specific regulatory processes across multiple studies of different therapeutic areas and phases, in accordance to appropriate regulations, Standard Operating Procedures SOPs, and study specific protocols/plans and processes. Clinical: Coordinate and participate in clinical research studies conducted by principal investigators at Duke University Medical Center; coordinate and participate in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Assist in the determination of guidelines for the collection of clinical data and/or administration of clinical studies. Coordinate and implement procedures to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources; code, evaluate and interpret collected data and prepare appropriate documentation; obtain blood samples, cultures, tissues and other specimens for laboratory analysis. Ensure compliance with protocol guidelines and requirements of regulatory agencies; identify problems and/or inconsistencies and Monitor patients' progress to include documentation and reporting of adverse events; recommend corrective action as appropriate. Evaluate and interpret collected clinical data in conjunction with principal investigators as appropriate; prepare oral presentations or written reports and analyses setting forth progress, trends and appropriate recommendations or conclusions. Confer with principal investigators to assist in developing plans for research projects and to discuss the interpretation of results; collaborate on the preparation of manuscripts for publication. Coordinate the development of forms, questionnaires and the application of research techniques; assist in writing procedures manuals for data collection and coding. Review journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in t
