Statistical Programming, Associate Director
Tasks
- Develop clinical study reports
- Ensure compliance with technical and regulatory requirements
- Lead statistical programming activities
- Manage clinical study programming delivery
- Support data commercialization activities
- Support regulatory submissions
Perks/Benefits
Skills/Tech-stack
CDISC | Clinical drug development | Drug development | Regulatory Submissions | SAS | Statistical programming
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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