Senior Clinical SAS Programmer (Woodcliff Lake, NJ)

Primary Responsibilities:
-Develop and validate SAS programs for clinical trials, including phase II & III studies
-Define and create ad-hoc reports for clinical research teams
-Review data analysis plans and compose analysis data specification documents
-Review clinical study protocols, statistical analysis plans (SAPs), and implement protocol SAP in statistical programming
-Develop and validate SAS programs for analysis datasets (ADS) and TLFs (Tables, Listing, and Figures)
-Perform statistical analysis and produce safety and efficacy TLFs
-Create efficacy and safety tables, listings, and graphs for submission and create graph output using SAS/Graph procedures

Qualifications:
-Bachelor's degree from accredited university, Computer Science, Statistics, and other quantitative majors preferred. Master’s/PhD is a plus
-7+ years experience in statistical analysis of clinical data with a biotech or pharmaceutical company highly preferred; SAS programming experience is required
-Strong interpersonal and communication skills
-Demonstrated ability to assess information, make timely decisions, and prioritize numerous tasks
-Ability to work independently within a team structure

Type: Long-term Contract