Job Details
Statistical Programmer II
6038
Posted: 23/12/2025
- £Competitive
- Home Based - Poland, Poland
- Permanent
Statistical Programmer II | Leading CRO | Remote or Hybrid (Warsaw) | Poland
An established, fast-growing CRO is expanding its statistical programming team and is looking for Statistical Programmer IIs to join from anywhere in Poland. The role can be fully remote or hybrid in Warsaw.
This is a specialist organisation known for delivering high-quality clinical programs, trusted client partnerships, and a flexible working culture. They are expanding across Europe and handpicking a team of highly skilled, top-tier Statistical Programmers. This is a rare opportunity to join a highly specialised, expert-driven team where your technical expertise is valued and your contributions make a visible impact.
Your role
As a Statistical Programmer II, you will perform hands-on statistical programming tasks and may lead programming efforts for assigned projects. You will work on datasets and TLGs for regulatory submissions, support clinical data cleaning, and provide guidance to less experienced programmers.
Key responsibilities include:
What we’re looking for
What’s on offer
Next steps: If this opportunity excites you, please apply now with your CV.
Not the right role? Contact Jo Fornaciari directly for a confidential discussion about other potential opportunities.
An established, fast-growing CRO is expanding its statistical programming team and is looking for Statistical Programmer IIs to join from anywhere in Poland. The role can be fully remote or hybrid in Warsaw.
This is a specialist organisation known for delivering high-quality clinical programs, trusted client partnerships, and a flexible working culture. They are expanding across Europe and handpicking a team of highly skilled, top-tier Statistical Programmers. This is a rare opportunity to join a highly specialised, expert-driven team where your technical expertise is valued and your contributions make a visible impact.
Your role
As a Statistical Programmer II, you will perform hands-on statistical programming tasks and may lead programming efforts for assigned projects. You will work on datasets and TLGs for regulatory submissions, support clinical data cleaning, and provide guidance to less experienced programmers.
Key responsibilities include:
- Developing, programming, and reviewing SDTM and ADaM datasets, aCRFs, define.xml, and related documentation
- Programming and validating TLGs for Clinical Study Reports, ISS, and ISE
- Performing CDISC-compliant checks and other QC/validation procedures
- Developing SAS programs for data integrity checks and study-specific monitoring reports
- Supporting maintenance and development of clinical trial data and reporting standards
- Mentoring and providing guidance to junior programmers
- Ensuring compliance with SOPs, WIs, and regulatory requirements
What we’re looking for
- Master’s or PhD in Statistics, Biostatistics, Mathematics, or Computer Science
- 2+ years of experience in clinical trial statistical programming or data analysis
- Hands-on experience with SDTM, ADaM, TLGs, and SAS
- Familiarity with clinical trial tools (e.g., InForm, Medidata Rave, DFdiscover)
- Strong attention to detail, problem-solving skills, and organisational abilities
- Ability to work independently and collaboratively within cross-functional teams
What’s on offer
- Remote or hybrid working in Poland
- Long-term role in a growing, independent CRO
- Exposure to a variety of studies and high-profile clients
- Supportive environment with opportunities for professional growth
- Competitive salary, benefits, and bonus
Next steps: If this opportunity excites you, please apply now with your CV.
Not the right role? Contact Jo Fornaciari directly for a confidential discussion about other potential opportunities.
Jo Fornaciari
Principal Consultant | Biometrics
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