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FDA Post-doctoral Fellow
Office of Biostatistics and Epidemiology/Center for Biologics Evaluation and Research (CBER)/US FDA
To develop innovative trial design and data analysis strategies for cancer clinical trials especially immunotherapy trials. Specifically, the goal of this project is two-fold:
• first, to develop innovative approaches to ensure adequate study power and reduce the risk of false-negative finding;
• second, to enhance IO trial efficiency and mitigate the occurrence of non-proportional hazards (NPH) patterns.
The participant will be involved in the development and application of novel, cutting-edge techniques for trial design and data analysis, especially immunotherapy trials and other oncology trials, as well as perform literature reviews, presentation of research results, and preparation of scientific manuscripts.
PhD or other doctoral degree in biostatistics or statistics. Candidates with prior postdoctoral training are also eligible to apply. Any individuals, including non-US Citizens, who have resided in the US for a total of three of the past five years are qualified to apply.