We're seeking a Principal R Programmer to join our team, responsible for designing, developing, and validating R programs for statistical analysis and reporting of clinical trial data.
Requirements
- Designing, developing, and validating R programs for statistical analysis and reporting of clinical trial data.
- Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods.
- Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines.
- Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs.
- Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge.
Benefits
- Various annual leave entitlements
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
