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Penumbra is seeking a seasoned SAS statistical programmer to support analysis and regulatory submission activities for clinical trials. Under supervision, you will develop analysis programs, create datasets, listings, tables and graphs, and mentor junior staff.
You will maintain CDISC standards (SDTM/ADaM/CDASH), work with biostatisticians and data managers, ensure QMS/GCP compliance, and participate in data warehouse management. Travel about 10% is expected.
Penumbra is seeking a seasoned SAS statistical programmer to support analysis and regulatory submission activities for clinical trials. Under supervision, you will develop analysis programs, create datasets, listings, tables and graphs, and mentor junior staff.
You will maintain CDISC standards (SDTM/ADaM/CDASH), work with biostatisticians and data managers, ensure QMS/GCP compliance, and participate in data warehouse management. Travel about 10% is expected.