Statistical Analyst
Location: United States
Position Type: Full-time
Job Duties:
- Develop SAS® programs to generate statistical analysis data sets, analyze
clinical trial data, produce and validate descriptive and inferential statistical tables, listings,
and graphs for clinical trial reports, regulatory submissions, and publications;
- Write general SAS application code and explore new technologies to improve the productivity
of statistical programming;
- Participate with Biometrics, Data Management, and clinical staff in the development and standardization
of case report forms, databases, edit checks, programs, and documentation; and
- Complete work within defined time frames ensuring deadlines are met, and balance concurrent
tasks and priorities.
Qualifications:
- Master's degree with minimum of two years of SAS programming experience in pharmaceutical
or contract research organization industries; and
- Considerable exposure to NDA submissions.
Travel: Minimal
To apply for this position, send your resume to: hr@medpace.com
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