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Sunday, April 20, 2008

Senior SAS Programmer / Team Leader - PRA International (Raleigh, NC)

Job Description

We are currently seeking experienced Statistical SASĀ® Programmers for our growing Analysis & Reporting teams in the following offices: Raleigh, NC (World Headquarters); Lenexa, KS (Kansas City suburb). Several levels are available -- including Team Leader positions. The Analysis Programmer provides statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. This person also provides statistical output for clinical study reports. The SAS Programmer will review clinical study protocols and case report forms, work with biostatisticians, writers and clinical staff to generate data summarization, analysis and reports; write and document programs; write command files; generate analysis databases in SAS; produce tables, listings and plots presenting data; review reports for consistency between text and tables; and perform ad hoc programming. As a Team Leader (Principal SAS Programmer), you will provide senior-level statistical programming support and validation of statistical analyses, datasets, tables, figures and listings. You will also serve as the Project Team Leader overseeing operational activities of the other Analysis Programmers. You will certainly have the opportunity to keep your technical programming skills sharp with hands-on work. However, you will also participate in the Analysis & Reporting team's implementation/testing of new software applications, the review and update of SOPs, and leading new business initiatives.

Qualifications

All candidates must possess a Bachelors degree -- however, an advanced degree (M.S. or Ph.D.) is preferred. As a successful candidate, you will possess a minimum of 2 years (SAS Programmer) or 5 years (Team Leader) SAS Programming work in a pharmaceutical company or CRO. Additionally, Team Leaders must have the demonstrated ability to plan, supervise, implement, and monitor the Statistical SAS Programming processes for multiple clinical trials.

Organization

PRA International provides employees the opportunity to work on complex, global trials that can change the course of medicine. For over 25 years, we have had a single mission - to become the best CRO in the drug development industry. Strategically aligned with leading pharmaceutical and biopharmaceutical companies worldwide, we provide clinical trial services and work on some of the most advanced drugs and biologics in development today .In addition to a unique professional challenge, PRA offers a pay-for-performance compensation philosophy, a commitment to professional development, and a culture that encourages work/life balance.

PRA International also offers:

  • Extended personal time off because we know you have a life outside of work
  • Competitive benefits plan
  • Flexible work schedules
  • Access to world-class therapeutic expertise unrivaled by any other CRO

URL: www.prainternational.com/careers.htm
Email: WaerhouseAimee [at] praintl.com

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