Key responsibilities:
1:Develop efficient tools to facilitate the clinical trial design.
2:Perform statistical assessment for complex clinical trial design.
3:Other ad hoc tasks as assigned by supervisor.
Qualification:
1: Master degree with strong statistical background
2: Be interested in statistical methodology and application in clinical trial.
3: Have strong statistical knowledge to support methodological research and application in clinical trial.
4: Be familiar with SAS and R coding to support statistical assessment and exploration.