Principal SAS Programmer & Clinical Trials Lead
Clinvia
Clinvia is seeking a Principal Statistical Programmer to lead data analysis and contribute to statistical analysis plans. This position requires a strong background in SAS programming and at least 8 years of experience in the Pharmaceutical/Biotech sector. The role will involve creating CDISC SDTM and ADaM files, as well as ensuring data quality and compliance for NDA submissions. Candidates should have a BS/MS in Statistics or a related field. #J-18808-Ljbffr Clinvia
Vacancy posted 5 days ago
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