Biostatistician/SAS Programmer
Job Summary
To support clinical studies and regulatory submissions, the full-time remote Biostatistician/SAS Programmer will design and analyze trials, develop SAS programs for data manipulation and reporting, and provide statistical consultation to cross-functional teams.
Key responsibilities
- Design and analyze clinical trials and observational studies in collaboration with cross-functional teams
- Develop and validate SAS programs for data manipulation, statistical analysis, and report generation
- Perform quality control checks on datasets and statistical outputs, ensuring compliance with regulatory standards
Required qualifications
- Master's or PhD in Biostatistics, Statistics, or a related field
- At least 3 years of experience in biostatistics or statistics
- Strong proficiency in SAS programming (Base, Macro, SQL, and Statistical procedures)
- Experience with clinical trial data and regulatory submissions (e.g., CDISC SDTM/ADaM standards)
- Knowledge of statistical methods such as regression, survival analysis, and mixed models
Complete Job Description
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