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Wednesday, January 30, 2013

Direct Client: Lead Clinical SAS Programmer-----Canton, MI-----6+months

Hi,

This is Sudheer from SAGE IT INC.

Hope you are doing great. Please send me your updated resume if you're interested for our direct client position.

 

Title: Lead 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
  • 2 + years leading a team of SAS Programmers
  • 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

 

Thanks & Regards,

 

Sudheer

Sage IT Inc | www.sageitinc.com |

2801 Network Blvd, Suite 507, Frisco, TX 75034

Phone: 972-996-0650 Ex 333

E-Mail: sudheer.divi@sageitinc.net

G talk: sudheer.itrecruiter333@gmail.com

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