GLOBAL HEADQUARTERS

4141 Parklake Avenue

                                                                                                                                     Suite 530, Raleigh, NC 27612

(919) 786-8200

Analysis Programmer

PRA International is a fast-growing, global clinical research organization with over 2500 employees worldwide.  For over 25 years, we have had a single mission - to become the best Contract Research Organization (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.

Becoming a global leader requires a complete and long-term commitment to providing our clients with the highest quality professionals.  That's where you can make a contribution...become a leader on our Analysis & Reporting team! 

PRA International is an organization that believes in promoting talent from within.  There is always room for advancement…along with many opportunities for professional development and education.  Our salary and benefits are extremely competitive – both with other CROs and pharmaceutical companies.  PRA strongly believes in the "pay for performance" philosophy…which includes 4 weeks of paid time off your first year and discretionary bonuses – just to name a few. 

SUMMARY

We are currently seeking experienced Clinical SAS® Programmers for our growing Analysis & Reporting team in these locations: Raleigh, NC; Lenexa, KS; Charlottesville, VA. 

Positions at the following levels are available: Analysis Programmer II, Analysis Programmer III, and Principal Analysis Programmer. 

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.

ACCOUNTABILITIES

The individual selected for this position 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. This person may also mentor new analysis programmers. 

QUALIFICATIONS

ü An undergraduate degree in IT or computer related field is required.

ü An advanced degree is preferred, but not required.

ü Minimum of 2 years work-related Analysis Programming experience in a clinical trial setting – especially in Phase II and/or Phase III studies.

ü Must have previous SAS® experience, be detailed-oriented, computer proficient in a Windows environment and possess superior interpersonal and organizational skills.

ü Experience working in a CRO (Contract Research Organization), pharmaceutical, or biotech company is required.

For consideration, please forward your resume to: WaerhouseAimee@praintl.com

Or you can visit our website at: www.prainternational.com/careers.htm

Posted 3/31/2008