Job Responsibilities:

1. Providing statistical support for pre-market registration clinical studies or post-market IST studies, including the description of the study’s statistical components, sample size calculations, and statistical analyses.
2. Responsible for reviewing the statistical analysis plans and conducting statistical analyses provided by vendors, ensuring the quality of the statistics.
3. Providing statistical monitoring for pre-market registration clinical studies or post-market IST studies, including regular analysis of data results, among other responsibilities;
4. Responsible for communicating statistical issues with external experts.

Job requirements:

1. Bachelor's degree or above in Statistics; preference given to candidates with experience in statistical analysis for clinical trials of oncology drugs.
2. At least 1+ year of experience in medical statistics;
3. Possessing strong communication and coordination skills, as well as the ability to analyze and solve problems;
4. Proficient in medical writing and literature retrieval, both in Chinese and English.