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- Tasks: Develop and validate statistical programs for clinical trials using SAS and R.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Why this job: Make a real impact on patient outcomes through innovative clinical research.
- Qualifications: Bachelor’s degree in relevant field and experience with SAS and R programming.
- Other info: Inclusive culture with opportunities for growth and development.
The predicted salary is between 40000 - 50000 ÂŁ 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. 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 and R 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.
- Experience with SAS and R programming, gained in 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.
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 a 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, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized 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, subsidized 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.
Study Lead Programmer in Reading employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Lead Programmer in Reading
✨Tip Number 1
Network like a pro! Reach out to current or former employees at ICON through LinkedIn or professional groups. 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 your SAS and R skills. Be ready to discuss specific projects you've worked on, especially those involving CDISC standards. Show us how your experience aligns with what we do at ICON!
✨Tip Number 3
Don’t just focus on technical skills; highlight your collaborative spirit! We love team players, so share examples of how you’ve worked with others to solve problems or improve processes in your previous roles.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows your enthusiasm for joining our diverse and innovative team at ICON.
We think you need these skills to ace Study Lead Programmer in Reading
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 experience with SAS and R, 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 research and how your background makes you a great fit for our team. Be sure to mention your interest in CDISC standards and your analytical mindset.
Showcase Your Team Spirit: We love collaborative team players! In your application, share examples of how you've worked effectively in teams, especially in fast-paced environments. This will help us see how you can contribute to our diverse culture.
Apply Through Our Website: For the best chance of success, make sure to apply directly through our website. This way, we can easily track your application and ensure it gets the attention it deserves!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your SAS and R Inside Out
Make sure you brush up on your SAS and R programming skills before the interview. Be prepared to discuss specific projects where you've used these tools, especially in a clinical trials setting. Highlight any challenges you faced and how you overcame them.
✨Familiarise Yourself with CDISC Standards
Since the role involves working with CDISC standards, take some time to understand SDTM and ADaM datasets. You might be asked about your experience with these standards, so having examples ready will show that you're serious about the position.
✨Prepare for Team Collaboration Questions
As a Study Lead Programmer, you'll need to work closely with other team members. Think of examples from your past experiences where you successfully collaborated with biostatisticians or other programmers. This will demonstrate your ability to work effectively in a multi-disciplinary environment.
✨Show Your Analytical Mindset
Be ready to discuss how you approach problem-solving and data integrity. Prepare to share specific instances where your attention to detail made a difference in a project. This will help convey your strong analytical mindset, which is crucial for this role.