Statistical Programming Associate Director
Tasks
- Apply SAS programming for analysis and documentation
- Deliver statistical programming aspects of clinical development
- Develop clinical study reports
- Ensure CDISC standards compliance
- Lead statistical programming activities for projects and studies
- Support regulatory submissions
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical drug development | Drug development | Regulatory Knowledge | Regulatory Submissions | SAS | Stakeholder management | Statistical programming | Technical Regulatory Knowledge
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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