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The webinar highlights the importance of clinical data managers during the conduct of a clinical trial and outlines the process of collecting, managing, analyzing, and reporting clinical trial data from study startup through study closeout. The webinar also discusses the relationship between clinical data managers and principal investigators, clinical research coordinators, and clinical research associates. Learning Objectives: Explain the importance of data management in clinical trials. Describe the roles and responsibilities of clinical data managers (CDMs) in clinical trials. Discuss the ways in which data managers interact with other clinical trial stakeholders such as clinical research coordinators (CRCs) and clinical research associates (CRAs). Presented by: Iris Rigor, MPH, CCRP - National Cancer Institute, NIH For access to the full webinar please visit: https://about.citiprogram.org/course/...