If you are an experienced statistical programmer who is comfortable moving between statistical leadership and hands on programming, this role offers the scope and responsibility to match your expertise. You will contribute at a senior level across the full clinical trial reporting lifecycle.
Requirements
- MSc in Statistics or a mathematics based degree with substantial statistical content
- Strong experience as a statistician in a CRO
- Broad experience across clinical trial phases and therapeutic areas
- Strong analytical and problem solving capability
- Clear written and verbal communication skills, including the ability to explain statistical concepts to non statisticians
Benefits
- Competitive Salary
- Home working allowance
- Flexible working hours
- 25 days Annual leave plus bank holidays
- Option to purchase additional days holiday
- Pension with Company matching
- Private medical Scheme with Bupa
- Free standard eye test every two years
- Employee Assistance Program
- 5, 10, 15 years of service recognition awards
- Death in service scheme
- Long Term Disability Insurance