生物统计师

Advanced knowledge of clinical study designs, common analysis methods, descriptive and inferential statistics
Good knowledge of statistical programming languages (including SAS), software, techniques, and processes
Knowledge in regulatory regulation in clinical trials
Strong collaborative skills and ability to work with a cross-functional team.
Manage study parameters and study design to provide efficient, effective and optimally-sized studies
Promote efficient, innovative and robust evidence generation processes
Interact with stakeholders as key contact with regard to statistical and contractual issues.