Job Summary
A company is looking for a Principal Statistical Programmer Consultant in Oncology.
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 and programming standards with CROs and vendors
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
- Experience as a senior statistical programmer in a FDA regulated environment
- BA/BS in computer science, statistics, or math; or MA/MS with 8 years of experience
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