Sr Analyst, Statistical Programming
USA IRV-17211 Redhill/MLE, United States
USD 119K-168K Senior-level Full Time
Tasks
- Collaborate on draft CRFs database specifications edit checks
- Create regulatory compliant SAS programs
- Develop analysis datasets specifications summary output
- Maintain program validation documentation
- Perform complex analysis for data requests
- Plan statistical programming execution
- Review validate statistical programs
Perks/Benefits
Skills/Tech-stack
Clinical data | Clinical data management | Clinical trials | Data Management | Data Validation | Edit checks | FDA | GCP | ICH | ISO | MS Office | SAS | Statistical programming
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Roles
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