Role Overview
Responsible for clinical research statistical design, statistical support during research, and statistical analysis plan. Performs various statistical analyses in real-time and visualizes daily statistical analysis.
What You Will Do
Design statistical analysis plans, participate in CRF design review, assist in drug randomization, and coordinate IDMC.
Why It Might Be a Fit
Requires strong logical thinking, writing skills, and ability to convert statistical analysis results into popular language.
Requirements
- Master’s degree or above in biostatistics, epidemiology, public health, etc.
- More than 5 years of experience in clinical I-III phase research statistical design and statistical analysis
- Proficient in SAS, R, STATA, SPSS, etc. statistical software
- Familiar with domestic and international clinical trial and statistical-related laws, regulations, guidelines, industry expert consensus, and CDISC-related knowledge and work experience
- Strong English reading and writing skills, and ability to use English for daily conversations and email communication
To apply for this job please visit linkedin.com.
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