88-50100108 Statistical Programmer Analyst
Tasks
- Build interactive dashboards for clinical trial monitoring
- Create regulatory submission packages for FDA filings
- Deliver modular scalable and reusable programming solutions with validation documentation
- Design develop and validate SAS macros for clinical reporting
- Develop statistical visualizations and diagnostic reports
- Ensure data integrity and traceability
- Implement and execute programming deliverables
- Lead development and review of SAS programs for clinical research
- Transform and integrate multi format data into validated analysis datasets
- Translate statistical analysis plans into executable code
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | CSV | Clinical data | Clinical trial | Clinical trial monitoring | Data Transformation | Data Validation | Data cleaning | Data integration | Data merging | Data traceability | Excel | FDA | Figures | Interactive dashboards | Listings | Oracle | R | Regulatory Reporting | SAS | SAS Macros | Statistical Analysis | Statistical Analysis Plan | Statistical Reporting | Tables
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
Regions
Countries
States
Cities
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