IT JOBS: {SAP JOBS USA:113660} Direct Client: Clinical SAS Programmer----Canton, MI-----6+ Months Contract.

Thursday, 7 March 2013

{SAP JOBS USA:113660} Direct Client: Clinical SAS Programmer----Canton, MI-----6+ Months Contract.

Hi,

This is Sudheer from SAGE IT INC.

Hope you are doing great. Please send me your updated resume if you're interested our Direct Client position.

Title: Clinical SAS Programmer
Location: Canton, MI
Duration: 6 Months +
Start Date: Immediate
Interview: Telephone followed by Webex/Skype

The candidates will be responsible for the implementation and execution of various programming needs for the company's clients in pharmaceutical industry.

Responsibilities include:

Provide programming needs to support client's requirements
Work closely with statistical personnel to provide definitions, documentation, and review of derived variables needed to produce planned tables, listings, and graphs (TLGs)
Generate tables, listings and graphs from clinical trial databases using SAS
Develop, program, verify, validate and maintain clinical trial databases and data entry screens using SAS and related software
Develop data and programming specifications jointly with other programmers
Design specific data presentations including creative summary tables, graphs and patient listings
Assist in preparing the data validation plan based on customers' needs
Review data management guidelines for computer edit/validation checks
Adherence to SOPs and programming standards

Requirements:
KNOWLEDGE & SKILLS:

Strong programming and logic skills
Hands-on with clinical trials and pharmaceutical development
8 years SAS programming, SAS Base, SAS Macro and thorough knowledge of clinical database structures
Ability to program data presentations, using programs such as SAS procedures
Sound experience with data and production of TLGs

EDUCATION & EXPERIENCE:

The candidates must have a Bachelors or Masters degree in computer science or related discipline
Minimum 8 years experience desired
Previous hands-on experience with CDISC and ADaM are essential prerequisites
Experience in table and CDISC validation
Attention to detail and data mining as needed for data review
Experience in the pharmaceutical or CRO industry is preferred
Excellent organizational and communication skills are required