Offer summary
Qualifications:
Masters in Statistics required, Minimum 5 years experience in Statistical Programming, Expert knowledge of scientific principles, Advanced SAS programming skills, Familiarity with ICH, ISO, and FDA standards.
Key responsabilities:
- Generate tables, listings, and graphs from clinical trial databases
- Lead study or small programming project teams
- Utilize System Development Life Cycle for programming deliverables
- Write specifications for SDTM standards
- Pool data sets for submissions