Clinical SAS Programmer
Our client has an immediate need for a Statistical Programmer who will be responsible for leading projects as well as being a strong individual contributor in both Clinical Development and Medical Affairs. In this position you will oversee other study team members on programming specifications as well as SAS programs and macros for clinical studies. You will also be responsible for ad-hoc statistical analyses, safety surveillance, and departmental data standards initiatives. This position requires extensive experience in SAS programming including at least 5 to 7 years of experience leading statistical programming initiatives, projects, and teams within the drug development industry (pharmaceutical, biotech, or CRO). Experience in database design as defined by CDISC is required. Strong knowledge of Base SAS, SAS/STAT, SAS Macro language and SAS SQL as well as programming experience for NDAs/BLAs with eCTD formatted NDA/BLA submissions is required. The ideal candidate should have a M.S. or B.S in Statistics, Mathematics, Computer Science, or a related field with knowledge of FDA, ICH and EMEA guidelines.
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