欢迎应届或非应届生物统计相关专业同学踊跃尝试。
邮箱：yujie.ma@excel-cro.com
电话：53834000-160
联系人： Sarah Ma
Responsibilities
Assists in study design and development of statistical section in clinical trial protocols
Assists sample size and statistical power calculations and randomization schedule generation
Attributes to development of statistical analysis plans including table shells design for individual studies
Supports data safety monitoring board (DSMB) or data monitoring committee (DMC) and clinical endpoints committee (CEC) regarding to statistics analysis
Participate in statistical support for CRF design, database development, data validation plan and blinded data review
Performs SAS programming to generate tables, listings, figures, and statistical analyses
Assists higher level biostatisticians for the project tasks
Conducts literature searches to support statistical team
Performs other duties assigned by supervisor
Qualifications
An advanced degree (Ph.D. or M.S.) in biostatistics, statistics or related field
Ability to deal with sensitive inquiries or complaints from clients or potential clients and to protect confidentiality
Good communication and interpersonal skills
Proficient working in a PC/Windows environment
A good command of English language if one’s native language is not English