Key Accountabilities

1.Participate in or contributes to protocol development (including study design, sample size calculation, randomization, and statistical analysis methodologies), case report form design and data collection

2.Develop and review statistical analysis plan, tables/listings/figures mock-ups, statistical analysis report and statistical section of clinical study report

3.Interact with clients as key contact with regard to statistical issues

4.Work with programming team to complete a project according to the requirements, QC/review the programming deliverables

5.May provide trainings to non-statistical peers with regard to statistical methodologies

Education

MS or PhD in Statistics, Math or Scientific Discipline

Language Skills

Competent in written and oral Chinese and English

Minimum Working Experience

Minimum 2 years Pharmaceutical/Biotech and CRO statistician/biostatistician experience.

Qualifications

1.SAS programming skills with SAS Base, SAS/Macros and SAS/Stat

2.Solid knowledge of experimental design, descriptive and inferential statistics both theoretically as well as applied in clinical trials

3.Ability to use professional concepts to achieve objectives in creative and effective ways

4.Good project management skills

5.Teamwork spirit

上班地址：长宁区仙霞路137号盛高国际大厦