Job Details
R Programmer - FSP
6092
Posted: 18/03/2026
- £Competitive
- Home Based - Romania, Hungary, Bulgaria or Poland, Romania
- Permanent
Statistical Programmer II / Senior Statistical Programmer | Global CRO – FSP | Permanent
Romania | Hungary | Bulgaria | Poland | Home Based
We are partnering with a leading global CRO to recruit a Statistical Programmer II / Senior Statistical Programmer to join their well-established FSP team. This role supports a key pharmaceutical client and offers the opportunity to contribute to complex clinical trials within a sponsor-dedicated model.
This is an excellent opportunity for a programmer with solid industry experience who is looking to further develop their technical expertise, including expanding their R programming skills.
What You Will Be Doing:
What You Will Need:
What’s in It for You:
What to Do Next:
If this opportunity is of interest, please apply now with your CV, as interviews are being arranged.
Not quite right?
Please contact Jo Fornaciari for a confidential discussion about other opportunities.
Romania | Hungary | Bulgaria | Poland | Home Based
We are partnering with a leading global CRO to recruit a Statistical Programmer II / Senior Statistical Programmer to join their well-established FSP team. This role supports a key pharmaceutical client and offers the opportunity to contribute to complex clinical trials within a sponsor-dedicated model.
This is an excellent opportunity for a programmer with solid industry experience who is looking to further develop their technical expertise, including expanding their R programming skills.
What You Will Be Doing:
- Supporting statistical programming activities across studies, from start-up through to final delivery
- Developing, validating, and maintaining statistical programs (primarily SAS, with some R) for data manipulation, analysis, and reporting
- Collaborating with biostatisticians to interpret study protocols, SAPs, and analysis requirements
- Producing high-quality statistical outputs, including tables, listings, and figures (TLFs)
- Performing quality control (QC) of programming deliverables to ensure accuracy and compliance
- Contributing to the preparation of submission-ready outputs and regulatory deliverables
- Supporting process improvements and efficiencies, including the use of R where applicable
- Working collaboratively within cross-functional teams in a sponsor-facing environment
What You Will Need:
- Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field
- At least 4 years of experience in statistical programming within a CRO or pharmaceutical environment
- Strong experience in SAS programming
- Working knowledge of R 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
What’s in It for You:
- 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
- Health insurance and well-being support
- Generous annual leave
- Country-specific benefits (e.g. childcare support, gym discounts, travel subsidies, and more)
What to Do Next:
If this opportunity is of interest, please apply now with your CV, as interviews are being arranged.
Not quite right?
Please contact Jo Fornaciari for a confidential discussion about other opportunities.
Jo Fornaciari
Principal Consultant | Biometrics
Apply for this role
Recruitment