Statistical Programmer II (Clinical SAS Programmer)
Tasks
- Coordinate study start-up documentation
- Create tables figures listings
- Develop and validate SAS programs
- Ensure 21 CFR Part 11 compliance
- Generate ADaM datasets
- Generate SDTM datasets
- Maintain SOP compliance
- Mentor junior team members
- Participate in process improvement initiatives
- Perform quality control checks
- Review programming specifications
- Support clinical trial programming
Perks/Benefits
- Career development opportunities
- Inclusive workplace
- Mentorship
- Remote friendly work structure
- Technical training support
Skills/Tech-stack
21 CFR | 21 CFR Part 11 | ADaM | CDISC | CFR Part 11 | Clinical data | Clinical data standards | Data Standards | ICH GCP | Part 11 | Quality Control | SAS | SDTM
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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