R Programmer
EU
July 6, 2026 at 9:17 AM
Join a leading global CRO within a well-established FSP model, supporting a key pharmaceutical client on complex, high-impact clinical trials. This is a strong opportunity for an experienced Statistical Programmer to deepen their expertise while gaining further exposure to R in a sponsor-dedicated environment.
Take a hands-on role across the full study lifecycle, from start-up to final delivery. You’ll develop and validate statistical programs (primarily SAS, with growing use of R), produce high-quality TLFs, and contribute to regulatory submissions. Working closely with biostatisticians and cross-functional teams, you’ll also support QC activities and drive efficiencies, including increased adoption of R.
- Bachelor’s or Master’s degree in Statistics, Mathematics, r-100">Computer Science, or a related field
- At least 4 years of experience in statistical r-100">programming within a CRO or pharmaceutical environment
- Strong experience in SAS r-100">programming
- Working knowledge of R r-100">programming (or willingness to develop further)
- Good understanding of clinical trial processes and regulatory requirements
- Strong attention to detail and problem-solving skills
- Ability to work independently while contributing effectively to a team
- Good communication skills and experience working in a collaborative environment
- Our client values the development and well-being of their employees, offering a supportive and inclusive environment focused on long-term career growth.
- Competitive salary
- Flexible, home-based working
- r-100">Health r-100">insurance and well-being support
- Generous annual leave
- Country-specific benefits (e.g. childcare support, gym discounts, r-100">travel subsidies, and more)
If this opportunity is of interest, please apply now with your CV, as interviews are being arranged.
Please contact Jo Fornaciari for a confidential discussion about other opportunities.