Title: *SAS Programmer*

Client: *Boehringer Ingelheim*

Location: *Ridgefield, CT*

*GC/Citizen*

Duration: *One year*

Local: *Highly preferred (must be able to attend a f2f interview)*



*- Advanced SAS Certification required *

*- Can be verified via the Public Registry of SAS Certified Professionals.*



*JD below:*



   - Develop and maintain datasets as per the CDISC (SDTM and ADaM)
   standards; Extract data from various databases;
   - Develop and maintan programs toanalyze the data and procudereports
   consisting of Tables, Listings and Graphs that are generated from the
   available databases;
   - Apply Programming Development Life Cycle (PDLC) principles;
   - Develop programs using SAS(Statistical Analysis Software) and SQL;
   - Perform Programming using SAS softwareanalyzing the clinical trial
   data to produce the outputs for the clinical trial report;
   - Prepare specifications and process flow diagrams, and develop
   programming code logic flowcharts;
   - Write specifications for the analysis datasets and report (Tables,
   Listings and Graphs) generation;
   - Prepare reports to assist management in problem analysis, and submit
   recommendations for solution;
   - Create primary and validation programs;
   - Develop, test, debug and deploy the programs in coordination with
   other line functions as per standard operating procedures (SOPs);
   - Maintain study documentation;
   - Document and revise system design procedures, test procedures, and
   programming standards;
   - Analyze user/customer needs and software requirements to determine
   feasibility of design within time and cost constraints;
   - Create analysis files (datasets), and reports Tables, Listings and
   Figures;
   - Consult with customers about software design, maintenance, enhancement
   and customization;
   - Store, retrieve, and manipulate data for analysis and reporting;
   - Expand or modify existing programs for efficiency and reusability; and
   - Work on other ad hoc tasks as assigned.
   - Skills:



   - 1 - 3 years Pharma experience supporting clinical trials Working
   experience for clinical data; Familiar with trial analysis Familiar with SAS



   - Education:



   - Bachelors' Degree or equivalant experience MS Biostat
      - Advanced SAS Certification required
      - can be verified via the Public Registry of SAS Certified
      Professionals.

------------------------------------------

Thanks & Regards




*Prahlad Kumar Gupta  Resource Manager-**Recruitments*
609-478-0027 (Cell)
12 Roszel Road Suite 204-C | Princeton, NJ 08540
prahla...@nea-consulting.com

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