Experienced I Statistical Programmer
Tasks
- Collaborate with cross functional teams and trial stakeholders
- Contribute to process improvement projects
- Create and verify reviewer guides
- Create verify and deliver CDISC compliant data packages
- Design and develop programs for clinical research analysis and reporting
- Develop and maintain trial programming activities
- Ensure compliance with clinical programming standards
- Perform verification of programming and reporting activities
- Support submission activities for clinical research
Perks/Benefits
- N/A
Skills/Tech-stack
Biostatistics | CDISC | Clinical trials | Data Modeling | Data Privacy | Data Quality | ICH GCP | Python | R | Report Writing | SAS | SAS programming | Statistical Analysis
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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