Connecting...

SAS Programmer II

  • Job type Contract
  • Salary Negotiable
  • Location Ridgefield, Connecticut
  • Sector Pharma & Biotech

SAS Programmer II - Contract

Start: 03/18/2019
End: 03/13/2020

Reason: Vacant Position
Department: BDM - PROGRAMMING
Job Category: Clinical and Scientific

This is the perfect role for someone who is transitioning into Life Sciences from an academic background! There are two openings within this group, and the team is open to seeing candidates with anywhere from 1-5 years of experience.

Duties:
Develop and maintain datasets as per the CDISC (SDTM and ADaM) standards;

Extract data from various databases;

Develop and maintain programs to analyze the data and produce reports 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 software analyzing 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:


3 - 5 years Pharma experience supporting clinical trials Working experience for clinical data;

Familiar with trial analysis Prior experience with SAS / R Prior experience with Python

Education:
Bachelors' Degree or equivalent experience MS in Comp. Science

MS Biostat/Statistics - Advanced SAS Certification preferred - can be verified via the Public Registry of SAS Certified

Sthree US is acting as an Employment Business in relation to this vacancy.