Providing expert-level statistical programming support, the full-time Senior Statistical Programmer Contractor will work remotely on a contract basis, focusing on clinical and device studies, regulatory submissions, and programming quality within the department. Key responsibilities Develop, validate, and maintain SAS programs to generate SDTM and ADaM datasets, as well as Tables, Listings, and Figures (TLFs) Provide statistical programming support for clinical and device studies, including CSRs and exploratory data analyses Collaborate with biostatistics, data management, and cross-functional teams to ensure compliance with regulatory standards and support various business initiatives Required qualifications 10+ years of hands-on statistical programming experience within the pharmaceutical, biotechnology, or CRO industry Expert-level proficiency in SAS programming, including advanced macro development Strong knowledge and practical experience with CDISC standards, including SDTM and ADaM Experience supporting regulatory submissions and clinical studies Familiarity with R and/or Python for statistical analysis is highly desirable
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