Developer II, SAS Programmer
About the role
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Developer II, SAS Programmer
Location: North Wales
Position Duties:
* Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
* As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
* Develop SAS programs for reports, analytics and data checks
* Develop SQL reports as needed
* Perform data mining on datasets as needed using SAS or SQL
* Database report server management as needed
* Execute database updates via system configuration as needed
* Database integration (images, clinical histories, other business databases)
* Prepare database queries
* Database maintenance
* Validation of programs and database systems and process
* Implement new softwares and techniques that can be used for reports and analytics.
* Acquire report requirements from users
* Demo reports to users
* Train users on reports
* Configure report subscriptions
* Travel (approximately 1%) domestic and/or international
Qualifications:
* Five years SAS programming required
* Two years Clinical trial experience preferred
* Data mining and Machine Learning experience preferred
* Knowledge of Python, R and Spotfire preferred
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
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11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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