Senior Statistical Programmer I
Tasks
- Collaborate with biostatisticians on analysis plans and statistical methods
- Develop validate SAS programs for clinical trial analysis and reporting
- Identify process improvements in programming practices and methodologies
- Perform quality control checks on statistical outputs
- Prepare statistical reports presentations and publications for regulatory submissions
Perks/Benefits
- Annual leave
- Employee assistance program
- Flexible optional benefits
- Health insurance
- Life assurance
- Retirement planning
Skills/Tech-stack
Clinical Trial Data | Clinical trial | Data Validation | Quality Control | Regulatory Compliance | SAS | Statistical Analysis | Statistical Reporting | Statistical programming | Trial data
Education
Bachelor of Engineering | Bachelor of Science | Master of Science
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