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Clinical Trials Regulatory Coord
Position SummaryThe Scientist participates in the development and writing of investigator-initiated clinical cancer trials and be the primary individual responsible for submission of these protocols (and their reports/renewals and related correspondence) to regulatory agencies (such as the US FDA). In addition, the Scientist oversees the performance and analyses of ancillary biological studies to achieve the scientific aims of those clinical trials, analyze collected lab and clinical data and serve as a co-investigator/co-author for publications related to these clinical trials. The overall aim of the clinical research initiatives in the Division of Pediatric Hematology, Oncology, and Bone Marrow Transplant (The Division) is to improve outcomes for children with cancer and non-


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