Principal Statistical Programmer

A company is looking for a Principal Statistical Programmer to support in-house projects. Key Responsibilities Participate in CRF design, database review, data management plan, and data validation procedures Produce data listings, summary tables, and graphics for analyses Coordinate data transfer with CROs and vendors, and validate analysis datasets Required Qualifications Minimum of 10 years of SAS programming experience in the pharmaceutical or biotechnology industry Expertise in SAS programming language and report generation Experience with CDISC data standards and therapeutic area of Oncology Experience as a senior statistical programmer in an FDA-regulated environment BA / BS in computer science, statistics, or math; or MA / MS with 8 years of experience