SAS positions

From sasCommunity

The following positions for SAS Programmers/Developers

1. Systems Programmer II: SAS PROGRAMMER – The client is seeking a SAS Programmer who will be involved in all phases of technical support and client coordination for the project. Responsibilities will include working within the implementation team, preparing documentation, interacting with state health agencies and interfacing with other development efforts. Specifically, the candidate will be responsible for, but not limited to, the following activities:
   • Learning those features of PHINMS necessary to guide its implementation by State and Territorial agencies
   • Development and maintenance of an implementation tracking process
   • Creating and disseminating guidelines for implementation to the reporting agencies
   • Phone and email consultation with regard to questions, problems, and needs of the reporting agencies
   • Documenting identified problems and reporting of issues experienced by reporting agencies
   • Written and oral reports on the status of the implementation project
   • Maintenance and revisions of existing underlying SAS or other database tables and stored procedures
   • Development and programming responsibilities to ensure successful transition of all or portions of legacy data to new systems
   • Documenting adjustments to ensure system performance and accuracy as necessary
   • Working closely with the implementation team in all phases, in a dynamic team oriented environment.
2. A SAS Programmer is needed to Update & maintain the Data warehouse and Generation of various Sales and Marketing & Pharmaceutical data analysis and generate Reports by making extensive use of Base SAS, SAS/Macros, and SAS/Reports on Unix. As a programmer analyst most of the work will involve the processing of clinical trials data. Most of this work requires analyzing / integrating data from many sources. The clinical trial data is made available to the SAS system. This data is to be collected on designing of phase I, II, III & IV.
   Responsibilities:
   • To perform preliminary data validation (clinical data check) using proc COMPARE of BASE SAS.
   • Creating Case Report Tabulations (CRT) for New Drug Application (NDA) using SAS/Macros for FDA submissions.
   • Creating SAS Views from tables in Oracle Data Base using Proc SQL.
   • Refreshing tables in Oracle Schemas with the SAS data sets.
   • Preparing analysis plans, data analysis and statistical report writing presentations to FDA.
   • Creating Kaplan-Meier survival curves using Proc Life test and Gplot.
   • Convert output into PDF files and MS-PowerPoint presentations.
   • Perform extensive Edit check programming using SAS/Base.
   • Used Proc REPORT to generate reports and involved in documenting experimental antibiotic drugs using SAS
   • Creating data entry screens using SAS FSP code.

    Environment: SQL, PL/SQL, SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL, and MS-Excel
   

Interested individuals please send your resumes to Jethro at jethro@techsoftgroup.com