Job Summary
A company is looking for a Principal Statistical Programmer to support in-house projects.
Key Responsibilities
- Participate in CRF design, database review, data management plan, and data validation procedures
- Produce data listings, summary tables, and graphics for analyses
- Coordinate data transfer with CROs and vendors, and validate analysis datasets
Required Qualifications
- Minimum of 10 years of SAS programming experience in the pharmaceutical or biotechnology industry
- Expertise in SAS programming language and report generation
- Experience with CDISC data standards and therapeutic area of Oncology
- Experience as a senior statistical programmer in an FDA-regulated environment
- BA/BS in computer science, statistics, or math; or MA/MS with 8 years of experience
Comments