Statistical Programmer II (SDTM)
Tasks
- Apply efficacy endpoint knowledge
- Contribute to process improvements
- Debug SAS macros
- Develop SDTM trial design domains
- Follow clinical programming standards and quality processes
- Perform quality focused SAS programming
- Prepare regulatory submission packages
- Program SDTM datasets
- Resolve data issues with cross-functional teams
- Review clinical study protocols and SAPs
- Support SDTM Leads deliverables
Perks/Benefits
Skills/Tech-stack
Analysis Plans | Clinical data | Clinical data standards | Clinical programming | Clinical programming standards | Clinical trial | Clinical trial protocols | Data Quality | Data Standards | IMWG | Programming Standards | RECIST | Regulatory Submission | SAS | SAS Macros | SDTM | SDTM mapping | Statistical Analysis | Statistical analysis plans | Trial Protocols | Trial design
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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