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Senior Statistical Programmer II

30+ days ago 2026/11/10
Other Business Support Services
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Job description

Senior Statistical Programmer

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.



As a Senior Statistical Programmer II at ICON, you will the analysis and reporting of clinical trial data, ensuring the integrity and accuracy of statistical outputs.


What You Will Do:


Your experience in statistical programming will be key in delivering high-quality outcomes and mentoring colleagues.
Key responsibilities include:


  • Designing, developing, and validating SAS programs for statistical analysis and reporting of clinical trial data.
  • Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods.
  • Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines.
  • Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs.
  • Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge.

Your Profile:


  • 10+ years of Clinical Programming experience with progressive responsibilities in clinical trials and strong expertise in SAS.
  • Expert knowledge of CDISC SDTM standards and hands-on experience with LSAF, clinical data review, data transformations, and regulatory deliverables.
  • Proven trial leadership experience, including leading programming teams, managing study deliverables, and driving successful project outcomes across Phase I–IV clinical trials.
  • Strong technical and analytical skills, including development of macros, edit checks, visualizations, and submission packages for global regulatory agencies.
  • Effective collaborator and mentor, with the ability to work cross-functionally, manage multiple priorities, and guide teams to deliver high-quality, compliant results.

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


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