Senior Statistical Programmer II
Tasks
- Collaborate with biostatisticians to create analysis plans and apply statistical methods
- Design develop and validate SAS programs for clinical trial analysis and reporting
- Mentor junior programmers and share best practices
- Perform quality control checks on statistical outputs
- Prepare statistical reports, presentations, and regulatory submissions
- Review statistical outputs for compliance with project specifications and regulatory guidelines
Perks/Benefits
- Disability coverage
- Employee Assistance programmes
- Health and Wellbeing Programmes
- Learning and development opportunities
- Life assurance
- Retirement and pension plans
Skills/Tech-stack
Analysis planning | Biostatistics | Clinical Trial Data | Clinical trial | Programming validation | Quality Control | Regulatory Compliance | SAS | Statistical Analysis | Statistical programming | Trial data
Education
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