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- Tasks: Develop and validate statistical programs for clinical trials using SAS.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Inclusive culture with opportunities for professional development and career growth.
- Why this job: Make a real impact on patient outcomes while growing your career in clinical programming.
- Qualifications: Bachelor’s degree in relevant field and foundational SAS knowledge.
The predicted salary is between 35000 - 45000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Ready to launch your career in clinical programming with an organisation that invests in your development and values your contribution? At ICON, we’re looking for a motivated Study Lead Programmer to join our diverse, collaborative, and forward-thinking team.
In this role, you’ll support the development and validation of statistical programs that drive high-quality clinical trial analysis and reporting. Your work will directly contribute to advancing clinical research and improving patient outcomes worldwide.
What You Will Be Doing
- Using SAS to support the development, validation, and maintenance of statistical programs used for data manipulation, analysis, and reporting in clinical trials.
- Working closely with senior statistical programmers and biostatisticians to interpret project requirements and contribute to Statistical Analysis Plans.
- Assisting with data cleaning, derivations, and quality checks to ensure data integrity prior to analysis.
- Participating in the creation of tables, listings, and figures (TLFs) and contributing to documentation for clinical study reports and regulatory submissions.
- Gaining hands-on experience with CDISC standards, with a particular focus on ADaM dataset development, including understanding specifications, traceability, and validation.
- Learning and applying relevant industry and regulatory standards (e.g., ICH/GCP) to ensure compliance and consistency across deliverables.
Your Profile
- Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related field.
- Foundational knowledge of SAS within a clinical trials setting.
- A keen interest in CDISC standards, with familiarity of SDTM and ADaM datasets.
- Strong analytical mindset, excellent attention to detail, and a proactive attitude toward learning and problem-solving.
- Collaborative team player with solid communication skills and the ability to work effectively in a fast-paced, multi-disciplinary environment.
- Knowledge of clinical trials, data management processes, or biostatistics is an advantage — but not essential. We’ll help you grow.
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:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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.
Study Lead Programmer employer: IRE
Contact Detail:
IRE Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Lead Programmer
✨Tip Number 1
Network like a pro! Reach out to current or former employees at ICON through LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by brushing up on SAS and CDISC standards. We recommend practising common programming scenarios and being ready to discuss how you've tackled challenges in past projects.
✨Tip Number 3
Show your passion for clinical research! During interviews, share why you're excited about improving patient outcomes and how your skills align with ICON's mission. It’s all about making that personal connection.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at ICON.
We think you need these skills to ace Study Lead Programmer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Study Lead Programmer role. Highlight your SAS experience and any relevant projects you've worked on in clinical trials.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about clinical programming and how your background aligns with our mission at ICON. Be genuine and let your personality shine through!
Showcase Your Analytical Skills: In your application, emphasise your analytical mindset and attention to detail. Share examples of how you've tackled challenges or solved problems in previous roles, especially in data management or programming.
Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at IRE
✨Know Your SAS Inside Out
Make sure you brush up on your SAS skills before the interview. Be prepared to discuss how you've used SAS in previous projects, especially in a clinical trials setting. Highlight any specific examples where your programming made a difference in data analysis or reporting.
✨Understand CDISC Standards
Familiarise yourself with CDISC standards, particularly SDTM and ADaM datasets. During the interview, show your enthusiasm for these standards and how they relate to the role. If you have any experience or coursework related to these, be sure to mention it!
✨Showcase Your Analytical Mindset
Prepare to demonstrate your analytical skills and attention to detail. Think of examples from your past experiences where you solved complex problems or improved processes. This will help convey your proactive attitude and readiness to tackle challenges in a fast-paced environment.
✨Be a Team Player
Since collaboration is key in this role, come ready to discuss how you've worked effectively in teams before. Share specific instances where your communication skills helped bridge gaps between team members or contributed to successful project outcomes.