Statistical Programmer

Planet Pharma; Poland; On-site; PLN 180,000 - 280,000; Full time

Benefits offered by this job

Remote work within Poland

Career progression in a growing center

Job summary

Planet Pharma in Poland is expanding its Statistical and Data Management Center of Excellence and is hiring Statistical Programmers for a fully remote role within Poland. This is an opportunity to contribute to high-quality regulatory deliverables and influence the direction of the team.

You will support clinical trial programming across multiple studies, working in a data-driven environment and collaborating with cross-functional teams, with mentorship and growth opportunities as the group

Qualifications

• Experience in clinical trial statistical programming.
• Hands-on SDTM/ADaM, CDISC, and P21 experience.
• Ability to lead study-level programming independently.

Responsibilities

• SDTM/ADaM development and dataset specification.
• CDISC-compliant programming and QC.
• Pinnacle 21 validation and issue resolution.
• Create and QC define.xml.
• Program and QC TLFs for CSR/ISS/ISE.
• Collaborate with biostatistics and data management teams.
• Lead programming workstreams and mentor others.
• Contribute to macro development and process improvements.

Skills

Clinical trial programming

Team leadership

Mentoring

Tools

SAS

CDISC

Job description

We are supporting a global research company that is currently in a major growth phase and expanding its statistical programming team in Poland. As part of this expansion, they are creating a Statistical and Data Management Center of Excellence. This is an opportunity to join early, influence the direction of the group, and work within a high‑quality, data‑driven environment.

They are looking for Statistical Programmers at varying levels to join on a remote basis within Poland. You will support clinical trial programming activities across multiple studies and contribute to high‑quality regulatory deliverables.

Key Responsibilities

• SDTM/ADaM development and dataset specification
• CDISC‑compliant programming and QC
• Pinnacle 21 validation and issue resolution
• Creation and QC of define.xml
• Programming and QC of TLFs for CSR/ISS/ISE
• Collaboration with biostatistics and data management teams
• Leading programming workstreams and mentoring
• Contributing to macro development and process improvement

Requirements

• Experience in clinical trial statistical programming
• Strong SAS programming skills (R experience is a plus but not required)
• Hands‑on experience with SDTM, ADaM, TLFs, CDISC, P21
• Prior experience in a CRO or pharma environment
• Ability to work independently and lead study‑level programming
• Based in Poland

What’s on Offer

• Join a team in a major growth phase
• Fully remote role within Poland
• Opportunity to help shape a new Center of Excellence
• Work across diverse therapeutic areas
• Strong focus on quality, collaboration, and innovation
• Clear progression opportunities as the team scales