Clinical SAS Programmer
Virtual Vocations Inc
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
Vacancy posted 6 hours ago
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