Key Skills: SAS programmer ,Research Scientist

Provide programming needs to support clients 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.
Requirements
KNOWLEDGE & SKILLS:
Strong programming and logic skills. Hands-on with clinical trials and pharmaceutical development. 2 to 4 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 2 to 4 years experience desired. Candidates with an Associate degree having strong programming background may also be considered. Experience in the pharmaceutical or CRO industry is preferred. Excellent organizational and communication skills are required.

Please send your resume and ensure to mention your salary history and current salary requirement when applying for this position.

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