Principal, SAS Programmer

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 to fulfil our mission to advance and improve patients’ lives.

Our ‘Own It’ 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’s our vision. We’re driven by it. And we need talented people who share it.
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 the friendliest people in the sector, and you’ll be helping shape an industry.

The Role
ICON is recruiting for Senior/Principal SAS Programmers with minimum 6 years experience in ADAM, TLFs and SDTM- Lead and execute programming deliverables on multiple projects in parallel and ensure that competing priorities are managed appropriately.
- Lead and manage the assigned programming team’s deliverables at the study level to ensure project objectives are met within budget, to agreed timelines and to the highest standard of quality.
- Proactively plan for and implement effective resource planning, task allocation and tracking of workload in accordance with agreed KPIs and quality standards.

or
- Develop, implement and maintain documentation to technically train staff in the appropriate technical solution.
- Actively participate in the review and approval of programming procedures and techniques.
- *Strive for excellence and act in a proactive and responsive manner to internal and sponsor needs.
- *Demonstrate a constructive and flexible approach to project delivery, including problem solving, handling changing priorities and meeting study timelines.
- *Proactively participate and contribute towards department goals, including sharing of extensive technical knowledge, current literature reviews and process improvement initiatives.
- *Preparation and delivery of presentations and attendance at appropriate scientific meetings and conferences.
- *Keep management informed of project status in relation to quality, timelines and/or performance issues.

You will need:
Bachelors or Master's degree in statistics, biostatistics, or related field
Minimum of 6 years of experience in the Pharmaceutical/CRO industry

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve 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 - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But 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.

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.

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