Senior Statistical Programmer (Oncology)
IQVIA · Durham, NC +1 more
BiometricsFull-time$88k–$221kCompany career page
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Role summary
IQVIA seeks a Senior Statistical Programmer to conduct SAS-based statistical programming for oncology clinical trials. The role involves generating CDISC-compliant datasets, implementing analyses per statistical analysis plans, and validating programming outputs while ensuring compliance with regulatory guidelines.
What they're looking for
- Bachelor's degree in mathematics, statistics, computer science, or health-related field
- 4–8 years of SAS programming experience in pharmaceutical industry
- Strong SAS programming skills with attention to detail
- Knowledge of regulatory guidelines and electronic submission standards
- Ability to manage multiple tasks and work under timeline pressure
- Strong organizational, communication, and project coordination skills
What you'll be doing
- Conduct statistical programming of clinical data using SAS software
- Generate analysis datasets according to CDISC standards and statistical analysis plans
- Produce summary tables, graphs, and data listings; conduct ad hoc analyses
- Validate programs and results from other programmers; review CDISC validation output
- Participate in table/listing/figure shell preparation and support statisticians with SAP development
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
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