To support clinical study design and analysis, the full-time Statistician will lead statistical input, develop statistical analysis plans, and deliver high-quality outputs using SAS while collaborating with global teams remotely. Key responsibilities Lead statistical input into clinical study design and analysis Develop statistical analysis plans, sample size calculations, and randomization schemes Deliver high-quality statistical outputs (TFLs) using SAS and contribute to Clinical Study Reports Required qualifications Degree in Statistics, Biostatistics, or a similar field 2+ years of working experience in CRO, pharma, biotech, or research Solid knowledge of clinical trials, GCP, and statistical methods Working experience with SAS Fluent in English and Taiwanese/Taigi
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