As an indispensable role in clinical trials, statisticians cover the entire life cycle of clinical trials, and will be exposed to statistical work in all stages of clinical trials, including participating in trial design, developing analytical methods, interpreting trial data, etc. Communicate and collaborate with all departments in clinical trials to ensure effective clinical development.
Job responsibilities
1. Write and review statistical analysis plan, table/listing/figure template and/or statistical analysis report;
2. Participate in study design, derive statistical methods, calculate the sample size and statistical power;
3. Develop randomization scheme and randomization tables, if applicable;
4. Review case report forms and other data management related documents, including but not limited to logic check specifications, data review plans, data transfer plans, etc.
Job qualification
1.Major in biostatistics or related, PhD, who would be expected to contribute to the statistical methodology development of clinical trials, simulations, and innovative research and development;
2.Familiar with SAS Base, SAS/Macros, SAS/Graph, SAS/Stat;
3.solid statistical knowledge;
4.good oral and written communication skills in Chinese and English;
5.good team work ability, problem solving, self-learning ability.