Senior Statistical Programmer II
Tasks
- Apply CDISC standards to datasets
- Create clinical study report content
- Develop statistical programming deliverables
- Ensure compliance with technical and regulatory requirements
- Lead analysis and reporting activities
- Manage stakeholders and study activities
- Perform statistical programming for clinical trials
- Support clinical study analysis and reporting
- Support regulatory submissions
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical trials | Regulatory Submissions | SAS | Stakeholder management
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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