Job Description

At ICON, it\xe2\x80\x99s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients\xe2\x80\x99 lives.

Our \xe2\x80\x98Own It\xe2\x80\x99 culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That\xe2\x80\x99s our vision. We\xe2\x80\x99re driven by it. And we need talented people who share it.
If you\xe2\x80\x99re as driven as we are, join us. You\xe2\x80\x99ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you\xe2\x80\x99ll be helping shape an industry.

The role:
We are the global biostatistics team dedicated to late phase research, working on (but not limited to) peri and post approval research, post authorization safety studies, observational and non interventional studies, patient reported outcomes as well as 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. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a client.

You will have strong demonstrable experience in:

• Designing, developing, validating and documenting SAS programs to generate analysis datasets, generate summary tables, figures and listings.
• Support statisticians in the development and review of Statistical Analysis plans and programming specifications
• Responsible for assisting data management with implementing protocols and CRFs

We are looking for:

• Bachelors or Master\'s degree in statistics, biostatistics, or related field
• SAS Programming experience \xe2\x80\x93 (ideally 3 yrs or more)
• Major experience in the Pharmaceutical/CRO industry

Benefits of Working in ICON:
Our success depends on the quality of our people. That\xe2\x80\x99s why we\xe2\x80\x99ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals \xe2\x80\x93 both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans \xe2\x80\x93 and related benefits such as life assurance \xe2\x80\x93 so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you\xe2\x80\x99ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is 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, because of a medical condition or disability, you need a reasonable accommodation 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.