Statistical Programmer II (FSP), POLAND

Remote from
Poland flag
Poland
Annual salary
Undisclosed
Salary information is not provided for this position. Check our Salary Directory to estimate the average compensation for similar roles.
Employment type
Full Time,
Job posted
Apply before
24 Oct 2025
Experience level
Midweight
Views / Applies
106 / 36

About Parexel

We help deliver life-changing treatments to patients around the world.

Verified job posting
This job post has been manually reviewed for authenticity and compliance.

When our values align, there’s no limit to what we can achieve.
At Parexel, we all share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.

Parexel is currently seeking a Statistical Programmer II to join us in POLAND, dedicated to a single sponsor.

Picture Yourself At Parexel:

The Statistical Programmer II provides technical expertise for the conduct of clinical trials and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of that role) on small, non-complex projects.

What You’ll Do At Parexel:

  • Deliver best value and high-quality service working on client system and following client processes

  • Work closely with client teams and Parexel colleagues in global environment

  • Specialize in one of the following therapeutic area: hematology/oncology/cell therapy

  • Use SAS programming to produce derived datasets (ADaM), tables, figures, and data listings of varying complexity

  • Develop and QC derived dataset specifications and other process supporting documents

  • Ensure all work maintains complete traceability and regulatory compliance

  • Participate and contribute to knowledge-sharing sessions with programming community

Requirements:

  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences

  • Minimum 3 years of SAS programming experience in clinical research

  • Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros

  • Strong understanding of CDISC standards

  • Knowledge of statistical terminology, clinical tests, and protocol designs

  • Excellent attention to detail with a focus on quality

  • Strong written and verbal English communication skills

A little about us:

Highly qualified and dynamic team. Multinational working environment. Smooth induction and training program. We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.

Parexel has a fully flexible work arrangement – you can be fully home based. But if you live close to our office in Warsaw and you want to use it, you are always welcome, and we will keep the desk ready for you!

Applicants must be authorized to work in Poland. We are unable to sponsor or take over sponsorship of an employment Visa.

Apply now >

Annual salary information is not provided for this position. Explore salary ranges for similar roles in our Salary Directory ›

This job listing has been manually reviewed by the Jobicy Trust & Safety Team for compliance with our posting guidelines, including verification of the company's legitimacy, accuracy of job details, clarity of remote work policy, and absence of misleading or fraudulent content.

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