Job Abstract
Participate in strategic planning and develop optimal clinical development plans with cross-functional drug development teams Oversee all the studies for one compound to ensure the consistency of statistical work standards as the project statistical leader Responsible for writing statistical methodology section of the protocol, including sample size calculation Responsible for writing statistical analysis plans (including mockup TL - Fs) for individual studies and ISS/ ISE Plan regulatory filing...
Search Terms: Director, Clinical Research, Regulatory, Experience