SAS Programmer Analyst

Intego Group is seeking for a SAS Programmer Analyst to join our team.

This high visibility role responsible for data manipulation, analysis and reporting of clinical trial data, including, but not limited to creation of analysis files, tables, listings, and figures, validation of those files, maintenance of associated tracking and validation documentation, and the creation and validation of CDISC SDTMs.

A majority of your work will be hands-on statistical programming, and you will be expected to perform complicated programming tasks quickly and efficiently.

Qualifications and Experience:

You will have a BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences or other related scientific subject, and a minimum 2 years of relevant career statistical programming experience in a clinical development environment.

Excellent SAS data manipulation, analysis and reporting skills:

• Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
• Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards
• Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
• Excellent oral and written English communication skills
• Ability to provide quality output and deliverables, in adherence with challenging timelines
• Ability to effectively perform complex statistical programming and related tasks
• Willingness and ability to provide guidance to team members on technical and process questions
• Strong ability to implement the latest CDISC SDTM, CDISC ADaM, and Define standards