Accountabilities:
1、Develops an******** appropriate statistical techniques for theanalysis of data in a statistical analysis plan.
2、 Design appropriate shells an******** for outputs. Performsstatistical analyses an******** results for clinical studies.
3、Develops or QCs analysis programs to implement techniquesdescribe******** the statistical analysis plan.
4、Approves final database for freeze/lock.
5、 Works with programmers, writers to coordinate data summarizationan******** act******** including summary stat******** tabulat********graph******** analysis output, an******** data listings.
6、Develops statistical reports an******** sections of clinical study reports.
7、Creates dummy an******** randomization schemes for clinical studies.
8、Participates in the development an******** of CRFs, data editspec******** an******** variable lists. Ma******** ******** an********knowledge of company an******** procedures an********.
9、Maintains sol******** of SAS procedures an******** programming practices.
10、Develops knowledge of FDA an******** guidelines an******** forreporting of clinical trials data.
Qualifications:
1、MS or PhD degree in statistics or biostatistics.
2、Demonstrates basic knowledge of b******** an********.
3、Shows basic understanding of clinical trial proce******** workflowsan******** systems.
4、Exhibits excellent written an******** communication skills;Read, writean******** English.