生物统计负责人

Major responsibility: • Operate in collaboration with study personnel to provide input to study protocol, perform sample size calculation, develop randomization schedule, write/review Reporting Analysis Plan, and write/review Statistical Analysis Report. • Participate in peer-review of work products from other statistical colleagues. • Oversee the process and quality of statistical work contracted out to CRO or research collaborator. • Collaborate with data management in the planning and implementation of data quality assurance plans. • Perform statistical programming to validate the results produced by CRO or to meet internal need of data analysis (e.g. for publication, or for optimizing assumptions for study design). Qualifications： • Educated to at least master level in Statistics, Math or equivalent field of study. • Positive working attitude. • Knowledge of statistical theories and application. • Knowledge of statistical tools such as SAS, nQuery, PASS, East. • Self-management skills with a focus on deliverables. • At least 8 years’ experience in pharmaceutical company or Clinical Research Organization (CRO) as a biostatistician or programmer. • Knowledge of early drug development and therapeutic areas such as respirology and infectious diseases.