| Provide statistically rigorous expertise including hands on development on study design, statistical analysis plans, communication of statistical results, project development plans, regulatory issues, and scientific and other product support projects; Accountable for timeliness and quality of study/... |
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Advanced degree in statistics or biostatistics; PhD preferred; A minimum of 8-12 years of experience in Pharma/Biotech designing phase 1-4 clinical trials, analyzing and reporting clinical trial data; A minimum of 8-12 years of experience in R and SAS programming including R packages, graphics (e.g.... |
