1. With supervision by a more senior statistician or head of Biostatistics, produces synopsis, statistical section of the protocol, and SAP for specific studies, statistical section of the CSR, as well as relevant part of CDP
2. With supervision by a more senior statistician or head of Biostatistics, computes sample sizes, discuss trial design, and creates randomization
3. In collaboration with the programmers, ensures that statistical programs are developed, tested and validated prior to the target analysis date; participates in programming activities (analysis files, TLFs, randomization...)
4. Reviews and approves study-related documents (CRFs, DEPs ...)
5. Provide statistical support to other statisticians as needed
6. Contribute to center development and efficiency improvement, or SOP development, or working groups/initiatives, as needed
7. Other duties as assigned by their manager.
REQUIREMENTS
At least PHD degree in statistics, or relevant field, overseas background is prefered.
Associate Statistician: 0-2 years of clinical trial experiences
Statistician: 1-3 years of clinical trial experiences
Senior Statistician: at least 3 years of clinical trial experiences
Good SAS knowledge and programming skills
Good understanding/experience working in a multidiscipline team of multi-culture company
Key competencies:
-Strong/effective English verbal and written communication skills
-Positive attitude, able to work effectively in a multi-cultural context as a good team player
-Strong problem solving ability, able to prioritize tasks, able to deliver quality work and results