Senior Statistical Programmer
Job Summary
Experienced professionals will find a full-time remote opportunity as a Senior Statistical Programmer, responsible for generating clinical trial data outputs using SAS, leading programming projects, and ensuring compliance with industry standards.
Key responsibilities
- Generate tables, listings, and graphs from clinical trial databases utilizing SAS programming
- Lead programming project teams and manage tasks to meet set objectives while providing guidance to junior colleagues
- Identify opportunities for improvement in service delivery and actively contribute to business development activities
Required qualifications
- Bachelor's degree in computer science or related field; Master's preferred
- 5-9 years of programming experience in the pharmaceutical or CRO industry
- Strong knowledge of drug development processes and clinical programming
- Proficient in SAS programming, including SAS Base and SAS Macros
- Thorough understanding of CDISC and HL-7 standards
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