Principal Statistical Programmer FSP
Tasks
- Collaborate with external and internal teams
- Create and validate programming standards
- Develop SAS programs for data analysis
- Develop and maintain programming tools and macros
- Ensure compliance with FDA regulations
- Generate SDTM and ADaM datasets
- Oversee CRO programming deliverables
- Participate in development of CRFs and data validation plans
- Review and author data transfer specifications
- Support clinical report and regulatory submission preparation
Perks/Benefits
Skills/Tech-stack
CDISC standards | Clinical Trial Methodology | Clinical trial | Data Analysis | Data Transfer Specification | Data Validation | Data transfer | Programming Standards | Project collaboration | R | Regulatory Compliance | SAS | Trial methodology
Education
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