Statistical Programmer II

Warman O'Brien; Województwo mazowieckie; Hybrid; PLN 150,000 - 210,000; Full time

Benefits offered by this job

Remote or hybrid in Poland

Competitive salary

Bonus potential

Job summary

Warman O'Brien in Poland seeks a Statistical Programmer II to own hands-on programming for SDTM/ADaM datasets, TLGs, and SDTM/ADaM datasets. You’ll work on regulatory submissions and contribute to data standards in a growing CRO.

You should have 3+ years in clinical trial programming, with SAS and familiarity with InForm and Medidata Rave. Remote or hybrid work options in Poland are available.

Qualifications

• Master's or PhD in Statistics, Biostatistics, Mathematics, or CS.
• 3+ years in clinical trial statistical programming or data analysis.
• Hands-on SDTM/ADaM/TLG and SAS experience.
• Familiar with InForm and Medidata Rave tools.

Responsibilities

• Develop, program, and review SDTM/ADaM datasets, aCRFs, define.xml.
• Program and validate TLGs for CSRs, ISS, and ISE.
• Perform CDISC-compliant QC/validation checks.
• Support development of clinical trial data and reporting standards.

Skills

Statistical programming

SDTM

ADaM

SAS

Teamwork

Education

Master's or PhD in Statistics

Tools

InForm

Medidata Rave

Job description

Statistical Programmer II | Leading CRO | Remote or Hybrid (Warsaw) | Poland

Take your statistical programming career to the next level by joining a fast-growing, expert-led CRO that’s expanding across Europe. This is a fantastic opportunity for a Statistical Programmer II to work on high-profile clinical studies, accelerate your development, and gain exposure to cutting-edge projects, all while benefiting from a competitive salary and flexible remote or hybrid working options in Poland.

In this role, you’ll take ownership of hands-on statistical programming across assigned studies, working on SDTM and ADaM datasets, TLGs, and regulatory submissions. You’ll play a key part in shaping clinical trial data and reporting standards, collaborating with experienced teams in a dynamic, growth-focused environment.

Key responsibilities

• Develop, program, and review SDTM/ADaM datasets, aCRFs, define.xml, and related documentation
• Program and validate TLGs for CSRs, ISS, and ISE
• Perform CDISC-compliant QC/validation checks
• Support development of clinical trial data and reporting standards

What we’re looking for

• Master's or PhD in Statistics, Biostatistics, Mathematics, or Computer Science
• 3+ years' experience in clinical trial statistical programming or data analysis
• Hands-on SDTM/ADaM/TLG and SAS experience
• Familiarity with clinical trial tools (e.g., InForm, Medidata Rave)
• Strong attention to detail, problem-solving, and teamwork skills

What’s on offer

• Remote or hybrid working in Poland
• Long-term role in a growing, independent CRO
• Opportunity to gain experience as the team expands across Europe
• Exposure to diverse studies and high-profile clients
• Competitive salary, benefits, and bonus