Senior Statistical Programmer I
Tasks
- Develop clinical study reports
- Ensure CDISC standard compliance
- Implement SAS programming for clinical development
- Lead analysis and reporting activities
- Perform statistical analysis and reporting
- Support regulatory submissions
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical Study Reporting | Clinical study | Clinical trials | Regulatory Submissions | SAS | Statistical programming | Study reporting
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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