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:
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