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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CompHealth exists to make the locums process easier. Not only will we search for jobs that fit your interests, we'll be here to handle all the details like credentialing, housing, travel arrangements, and so much more. So, relax and get back to helping patients, and let...