| Provide statistical consulting to clinical study design; Review study protocols and write statistical sections; Conduct sample size and power calculations; Propose randomization methods and designs; Lead regulatory submission strategy planning for statistics function; Identify issues, and provide so... |
|
Master’s degree with 6-10 years or Doctoral degree with 4-8 years of relevant experience in a health sciences research institute or the pharmaceutical/biotech industry; Direct participation in design, planning, conduct, analyses, and reporting of clinical trials; Direct participation in regulatory... |
