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Description
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.
Audience
Clinical Data Managers, Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Investigators, Research Administrators, Sponsors, Students
Meet the Presenter
Iris Rigor, MPH, CCRP – National Cancer Institute, National Institutes of Health
Iris Rigor has served as Lead Clinical Data Manager and Senior Clinical Research Project Manager for a vast portfolio of oncology and infectious disease clinical trials. She has also taught Clinical Trials Management courses, delivering fundamental training to students seeking to enter the clinical trials workforce.
