About this role

Study Lead 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 I at ICON, you will analyse clinical trial data and support the statistical analysis process to ensure high-quality results.

What You Will Do:

You will lead on statistical programming tasks requiring technical depth, with a focus on quality and continuous improvement.

Key responsibilities include:

  • Developing and validating programs for statistical analysis and reporting of clinical trial data, using R and SAS.

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

  • Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting.

  • Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions.

  • Contributing to process improvements by identifying efficiencies in programming practices and methodologies.

Your Profile:

You will have a strong foundation in statistical programming, with the experience to work independently and guide others.

Required qualifications and experience:

  • Bachelor's degree in statistics, computer science, mathematics, or a related discipline

  • Experience in statistical programming, preferably in a clinical research or pharmaceutical setting.

  • Strong proficiency in SAS and R programming, with a solid understanding of statistical concepts and methodologies.

  • 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 requestΒ here.

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

Frequently Asked Questions

Is the salary disclosed for the Study Lead Programmer position at icon?
The salary for this Study Lead Programmer role at icon is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Study Lead Programmer position at icon located?
This Study Lead Programmer role at icon is based in Bulgaria, Sofia, Estonia, Tallinn, Germany, Frankfurt, Hungary, Budapest, Kenya, Poland, Warsaw, Romania, Bucharest, Slovakia, Bratislava, South Africa, Johannesburg, UK, Reading. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Study Lead Programmer role at icon full-time or part-time?
This is listed as a Full time position. It is posted as a Study Lead Programmer role in the 168 ICON Clinical Research Poland sp. z.o.o. department at icon.
Which team or department does the Study Lead Programmer at icon belong to?
This Study Lead Programmer position is part of the 168 ICON Clinical Research Poland sp. z.o.o. department at icon. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Study Lead Programmer position at icon?
Click the "Apply Now" button on this page. You will be redirected to icon's official application portal hosted on workday where you can submit your application directly.
When was the Study Lead Programmer job at icon posted?
This Study Lead Programmer position at icon was posted on Jul 29, 2026. Apply as soon as possible β€” early applications are often reviewed first.
Study Lead Programmer
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