Join ICON: Be a Part of Transformational 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 fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. These values bring us together as individuals and set us apart as an organization.

We aim to be the Clinical Research Organisation that delivers excellence to our clients and patients at every touchpoint. In short, we strive to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share this vision.

Why Work With ICON?

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and friendliest people in the sector. Join us in shaping a transformative industry.

The Role: Sr Statistical Programmer II

We are part of a global biostatistics team dedicated to late-phase research. Our work includes, but is 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 Sr Statistical Programmer II, you will be responsible for statistical aspects of clinical and preclinical research projects. Your duties will include study design, case report form development, analysis planning and scheduling, data analysis, interpretation, and result reporting. You may also need to coordinate analysis efforts across multiple research projects for a client.

Your Responsibilities:

• Design, develop, validate, and document SAS programs to generate analysis datasets, summary tables, figures, and listings.
• Support statisticians in the development and review of Statistical Analysis Plans and programming specifications.
• Assist data management with the implementation of protocols and Case Report Forms (CRFs).

Qualifications:

• Bachelor’s or Master’s degree in statistics, biostatistics, or a related field.
• 3+ years of SAS Programming experience.
• Extensive 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. Some of the benefits include:

• Highly competitive salary packages, benchmarked regularly against our competitors.
• Annual bonuses reflecting the delivery of performance goals – both ours and yours.
• A comprehensive range of health-related benefits for employees and their families.
• Competitive retirement plans and related benefits such as life assurance.

Beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil 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 regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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

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Company name: ICON

Job title: Sr Statistical Programmer II