2 years of experience in each of the following Grant Development, Methodological Support of all facets of clinical research, Data analysis, and Scientific Publications. 2 years of experience with Phase I and Phase II clinical trials and Bayesian adaptive design, Basket design, in dosetoxicity and doseresponse studies. 2 years of experience in developing new methods or new applications for existing methods and new research, independently or collaboratively with other methodologists and presenting in regional or nationalinternational conferences in biostatistics, epidemiology, clinical trials, or public health. 1 year of experience participating in grant writing as a collaborator with the principal investigator and writing the statistical considerations section of a grant or a statistical core for larger grants such as program projects or center grants. Submission of at least one manuscript as a first or contributing author.
Categories: eb3
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