A company is looking for a Senior Statistical Programmer to support in-house projects. Key Responsibilities Participate in CRF design, database review, data management planning, and data validation procedures Produce data listings, summary tables, and graphics for analyses Coordinate data transfer and programming standards with CROs and vendors, and validate analysis datasets Required Qualifications Minimum of 10 years of SAS programming experience in the pharmaceutical or biotechnology industry BA / BS in computer science, statistics, or math, or MA / MS with 8 years of experience Expertise in SAS programming language and CDISC data standards Experience in an FDA-regulated environment and with Clinical Study Reports Ability to manage multiple tasks and meet project deadlines
Senior Programmer • Houston, Texas, United States