Clinical SAS Programmer Job in New Brunswick 08818, New Jersey US
We are actively recruiting for a Clinical SaS Programmer/Biostat for a top pharmaceutical company in the New Brunswick NJ area.
· Experience in SAS Programming and Biostatistical analyses for clinical trials in the pharmaceutical or biotechnology industry. At least 4 years of programming experience in a CRO, Pharma, or biotech company, of which at least two years in oncology (solid tumor studies). Experience in supporting ISS/ISE and NDA submission a major plus.
· Bachelor degree or higher in mathematics, statistics, computer science, physics or related quantitative field preferred.
· Familiar with CDISC conventions, such as SDTM and ADaM models and hands on experience implementing these models.
· Attention to detail. Analytical and logical approaches to tasks. Expertise in the production and reviewing of datasets, analyses, tabulations, graphics and listings from clinical trial data
· Strong DATA step programming skills. Experience with ODS, Base SAS, SAS/STAT, SAS/GRAPH, PROC REPORT, SAS Macro language. Experience working with EDC data sets.
· Solid understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
· Good organizational and communication skills, the ability to work in a collaborative environment
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