SAS Clinical Trial Programmer Position Summary: The SAS Clinical Trial Programmer supports all phases of clinical trial data analysis, from preparation to final submission, ensuring data accuracy and reliability. Key Responsibilities: Develop, validate, and maintain SAS programs for clinical trial analysis. Support biostatistics teams with efficient, reproducible code. Contribute to regulatory submission documentation. Qualifications: Bachelor's in a technical field; Master's preferred. Minimum of 2 years in clinical programming. Deep understanding of clinical trial methodologies and SAS programming. NavitsPartners
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