The specific duties for this position may include protocol development, study design, analysis plan, sample size/power calculations, and interpretation of study data; develop, design and write new and/or revised statistical programs (say in SAS or R) and modeling based on requirements of ongoing res... |
|
Master's degree in biostatistics, statistics or related quantitative field with 6+ years’ experience in design, conduct, monitoring, and analysis of cancer clinical studies, in preparing and reviewing clinical trial protocols, and in preparing grant applications and writing research reports, or do... |