ICON

Senior Statistical Programmer

Poland · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

EmployerICON
LocationPoland
Work styleWork style not stated
Employment typeFull time
Employer posted24 Aug 2026

Senior Statistical Programmer - R

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are currently seeking a Senior Statistical Programmer to join our diverse and dynamic team. As a Senior Statistical Programmer at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs in R, collaborating with biostatisticians, and ensuring compliance with regulatory standards.

What You Will Be Doing:

Show full description

Developing and validating R programs for statistical analysis and reporting of clinical trial data.

Leading more than one Statistical Programming team to create, validate and generate statistical outputs, including listings, tables, figures, and CDISC-compliant SDTM and ADaM datasets (including mapping specifications) of low to moderate complexity.

Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.

Performing quality control and validation of statistical outputs, ensuring accuracy, consistency, and regulatory compliance.

Assisting in the preparation of statistical reports, presentations, and publications to support regulatory submissions and clinical study reporting.

Contributing to process improvements by identifying efficiencies in programming practices, automation, and the use of R-based analytical workflows.

Supporting the development, maintenance, and enhancement of standardized R programming tools, macros, and reporting solutions across studies.

Your Profile:

Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related quantitative field.

Experience in statistical programming within a clinical research, biotechnology, or pharmaceutical environment.

Strong proficiency in R programming, including the development and validation of clinical trial datasets, analyses, and reporting outputs.

Good understanding of CDISC standards, including SDTM and ADaM, and their application within clinical trials.

Familiarity with regulatory requirements and industry guidance related to statistical programming and clinical data reporting.

Excellent analytical and problem-solving skills, with a keen attention to detail.

Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

See how well you match this job Apply on the employer’s site ↗

Check your resume against this job Free, no sign-up. Nothing you paste is stored.

Staying safe while you apply

Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

Check the fit.
Compare the requirements with the experience you have confirmed, including gaps.
Prepare honestly.
Build interview stories and application drafts from your own evidence.
Keep track.
Save the role and record your own application status and follow-ups.

Create a free workspace or log in.