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88,000+ live jobsRemote, South Africa, Johannesburg·Added 7 months ago
This job was published 7 months ago
Permanent contract
Per the ad.
Fully remote
Per the ad.
Have the right to work in Spain
ICON plc doesn't mention sponsorship in the ad.
University degree
“Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.” — per the ad.
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.
Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.
Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.
Exceptional analytical and problem‑solving abilities, with meticulous attention to detail.
Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.
Senior Statistical Programmer - Client Based
We're looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward‑thinking team. At ICON, you'll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision‑making in global healthcare.
In this role, you'll take ownership of developing and validating high‑quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards. Your expertise will directly support the success of our clinical studies and the advancement of life‑changing therapies.
Designing, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.
Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.
Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.
Supporting the creation of statistical reports, presentations, and regulatory submission documentation.
Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.
As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
Visit our careers site to
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
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Blue Card threshold🇬🇧€48k - €64k
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