Job Details
Senior Statistical Programmer I
6039
Posted: 23/12/2025
- £Competitive
- Home Based - Poland, Poland
- Permanent
Senior Statistical Programmer I / II | Leading CRO | Remote or Hybrid (Warsaw) | Poland |
An established, fast-growing CRO is expanding its statistical programming team and is looking for Senior Statistical Programmers to join from anywhere in Poland. The role can be fully remote or hybrid in Warsaw.
This is a growing organisation known for high-quality clinical deliverables, strong client relationships, and a flexible working culture. They are expanding across Europe and handpicking a team of elite, top-tier Statistical Programmers. This is a rare opportunity to join a highly specialised, high-performing organisation where your expertise is recognised, valued, and central to the company’s continued success. Work at the forefront of clinical research, make a lasting impact, and advance your career within a selective, expert-driven environment.
Your role
You will take a senior, hands-on role in statistical programming, leading projects and supporting regulatory submissions. You will also mentor junior programmers and help maintain programming standards.
Key responsibilities include:
What we’re looking for
What’s on offer
What to do next: If this opportunity is of interest, please apply now with your CV.
Not what you are looking for? Please contact Jo Fornaciari directly to arrange a confidential discussion about other potential opportunities.
An established, fast-growing CRO is expanding its statistical programming team and is looking for Senior Statistical Programmers to join from anywhere in Poland. The role can be fully remote or hybrid in Warsaw.
This is a growing organisation known for high-quality clinical deliverables, strong client relationships, and a flexible working culture. They are expanding across Europe and handpicking a team of elite, top-tier Statistical Programmers. This is a rare opportunity to join a highly specialised, high-performing organisation where your expertise is recognised, valued, and central to the company’s continued success. Work at the forefront of clinical research, make a lasting impact, and advance your career within a selective, expert-driven environment.
Your role
You will take a senior, hands-on role in statistical programming, leading projects and supporting regulatory submissions. You will also mentor junior programmers and help maintain programming standards.
Key responsibilities include:
- Leading statistical programming activities across clinical studies
- Developing, programming, and reviewing SDTM and ADaM datasets
- Programming and reviewing TLGs for CSRs, ISS and ISE
- Performing CDISC and Pinnacle 21 checks
- Preparing and reviewing define.xml, aCRFs, and related documentation
- Supporting regulatory submissions
- Improving processes, macros, and programming standards
- Mentoring and guiding less experienced programmers
What we’re looking for
- Degree in Statistics, Biostatistics, Epidemiology, Computer Science, or similar
- 6+ years of experience in clinical trial statistical programming
- Strong hands-on experience with SDTM, ADaM, TLGs, and CDISC
- Solid SAS programming skills
- Experience working in a CRO or pharmaceutical environment
- Comfortable leading workstreams and collaborating with cross-functional teams
- High attention to detail, good organisation, and a practical approach to problem-solving
What’s on offer
- Remote or hybrid working in Poland
- Long-term role in a growing, independent CRO
- Exposure to varied studies and clients
- Supportive environment with room for professional development
- Generous salary, benefits and bonus
What to do next: If this opportunity is of interest, please apply now with your CV.
Not what you are looking for? Please contact Jo Fornaciari directly to arrange a confidential discussion about other potential opportunities.
Jo Fornaciari
Principal Consultant | Biometrics
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