SAS Programmer III (JOB ID- 4715739)

Artech LLC.; Swiftwater (Monroe County); On-site; USD 80,000 - 120,000; Full time

Job summary

A leading IT staffing company is seeking a Statistical Programmer to provide programming support for statistical analyses and reporting of clinical studies. The ideal candidate will have expertise in SAS software, excellent programming skills, and a minimum of a master's degree in Statistics, Biostatistics, or Mathematics. The role requires 3-9 years of experience in the pharma or vaccine sector and involves developing new tools and performing various analyses as needed.

Qualifications

• Expertise in SAS software, especially Base SAS, SAS/Stat, and SAS/Graph.
• Excellent programming skills with regulatory submission experience.
• 3-9 years of experience in pharma or vaccine-related projects.

Responsibilities

• Provide programming support for statistical analysis and reporting.
• Assist in developing new tools or applications.
• Perform ad hoc analysis as required by project teams.

Skills

Knowledge of SAS software

Programming in FORTRAN

Programming in C++

Programming in Visual Basic

Programming in Oracle

Education

M.S in Statistics

M.S in Biostatistics

M.S in Mathematics

Tools

SAS

Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Job Description

The Statistical Programmer is responsible for providing significant programming support to the statisticians as part of the contribution towards the completion of statistical analyses (tables, listings and figures) and reporting of results of clinical studies. It includes Safety, Immunogenecity and Efficacy Analysis. In addition, other ad hoc analysis may have to be performed, based on the need, such as, analysis for Annual Reports, Publications, Information Brochure, Sales Aids, Poster Presentations, VRBPAC, CR and IR letters from regulatory agencies such as FDA, Drug Safety Monitoring Board (DSMB), exploratory analysis and other miscellaneous analysis as required by project/study teams. Assist in developing/building new tools or applications, developing and implementing new standards. Skills:

Knowledge of SAS software, including macros programs development, and awareness of current features in SAS, especially in Base SAS, SAS/Stat and SAS/Graph. Knowledge of additional programming languages, such as, FORTRAN, C ++, Visual Basic, Oracle, etc., would be a plus. Aptitude for "Look and feel for software" would be desirable. Requires excellent programming skills, experience with regulatory submission (NDA, eBLA/BLA, CTD/eCTD), and the ability to work in a multidisciplinary team. 3-9 years of pharma or vaccine experience

Education:

at least a M.S in Statistics, Biostatistics, Mathematics or a related field