Senior Statistical Programmer II
Tasks
- Apply CDISC standards to clinical data
- Collaborate with global teams on concurrent studies
- Develop statistical programming deliverables
- Lead clinical study report development
- Prepare regulatory submission programming activities
- Provide stakeholder management for oncology submissions
- Support analysis and reporting for clinical studies
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical data | SAS
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Roles
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