Join ICON: Your Future in Clinical Research

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us fulfill our mission of advancing and improving patients' lives. Our 'Own It' culture, driven by our core values – Accountability & Delivery, Collaboration, Partnership, and Integrity – unites us as individuals and sets us apart as an organization.

We aspire to be the Clinical Research Organization that consistently delivers excellence to both our clients and patients at every touch-point. In short, we aim to be the partner of choice in drug development. That’s our vision. We’re driven by it, and we seek talented individuals who share this passion.

Work with Us

If you’re as driven as we are, join us at ICON. You'll be part of a dynamic and supportive environment, working alongside some of the brightest and friendliest professionals in the sector, with the opportunity to help shape an industry.

The Role: Senior Statistical Programmer I

We are the global biostatistics team dedicated to late-phase research, working on (and not limited to) peri and post-approval research, post-authorization safety studies, observational and non-interventional studies, patient-reported outcomes, and analyses for abstracts, papers, and manuscripts.

As a Senior Statistical Programmer I, you will be responsible for the statistical aspects of clinical and preclinical research projects. Your project responsibilities will include:

• Study design
• Case report form development
• Analysis planning and scheduling
• Analysis and interpretation of data
• Reporting of results

You may also be required to coordinate analysis efforts across multiple research projects conducted for a client.

Skills and Experience

You will have strong demonstrable experience in:

• Designing, developing, validating, and documenting SAS programs to generate analysis datasets, summary tables, figures, and listings
• Supporting statisticians in the development and review of Statistical Analysis Plans and programming specifications
• Assisting data management with implementing protocols and CRFs

Qualifications

• Bachelor's or Master's degree in statistics, biostatistics, or a related field
• SAS Programming experience – ideally 6 years or more
• Significant experience in the Pharmaceutical/CRO industry

Benefits of Working at ICON

Our success depends on the quality of our people. That’s why we prioritize building a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages, regularly benchmarked against our competitors. Our annual bonuses reflect the delivery of performance goals – both ours and yours. We also provide a range of health-related benefits for employees and their families, competitive retirement plans, and related benefits such as life assurance, so you can save and plan for the future with confidence.

Beyond competitive salaries and comprehensive benefits, you’ll thrive in an environment where you are encouraged to fulfill your sense of purpose and drive lasting change.

Equal Opportunity Employment

ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

If you require a reasonable accommodation due to a medical condition or disability in order to participate in the application process or perform the essential functions of a position, please let us know through the form below.

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Company name: ICON
Job title: Senior Statistical Programmer I