Start your statistical programming career at ICON. Entry-level role: develop & validate SAS/R programs for clinical trial data. Statistics/CS degree & foundational SAS/R skills required.
Launch Your Career in Data Science for Clinical Development
At ICON, we are pioneers in clinical development, dedicated to turning scientific discovery into life-changing therapies. The power of data is at the heart of every breakthrough, transforming raw clinical trial data into clear evidence that supports regulatory decisions and patient care.
We are seeking a motivated and analytically minded Statistical Programmer I to join our Biometrics team. This is an entry-level role designed for recent graduates or early-career professionals eager to build a foundational career in statistical programming within the pharmaceutical industry. You will receive structured training and mentorship to develop and validate programs (primarily in SAS) that clean, analyze, and report clinical trial data. If you have a passion for data, a keen eye for detail, and a desire to contribute to meaningful science, this is your gateway to a rewarding career.
Your Mission: Build the Foundation for Reliable Clinical Data Analysis
As a Statistical Programmer I, you will work under the guidance of senior programmers and biostatisticians to learn the craft of clinical programming. Your work will support the creation of accurate datasets and outputs that are essential for understanding treatment efficacy and safety.
Key Responsibilities
1. Foundational Programming & Data Preparation
- Assist in developing, validating, and maintaining statistical programs using SAS (primary) or R to support data manipulation and analysis for clinical trials.
- Perform data cleaning, transformation, and quality control checks to ensure the integrity and accuracy of analysis datasets.
- Learn and apply CDISC standards (SDTM, ADaM) under supervision to structure data for regulatory submissions.
2. Collaborative Project Support
- Collaborate with senior statistical programmers and biostatisticians to understand project requirements and contribute to the execution of Statistical Analysis Plans (SAPs).
- Participate in team meetings and code review sessions to build your skills and ensure programming quality.
- Support the preparation of programming documentation and outputs (e.g., tables, listings, figures) for clinical study reports.
3. Learning & Professional Development
- Learn and adhere to industry standards, including ICH-GCP guidelines, ICON SOPs, and best practices in statistical programming.
- Gain familiarity with clinical trial data management processes and the drug development lifecycle.
- Develop problem-solving and analytical skills in a real-world, supportive environment.
Who You Are: The Ideal Foundation Builder
You are a recent graduate or early-career professional with a strong academic foundation in quantitative sciences. You are curious, detail-oriented, and excited by the prospect of applying your technical skills to impactful healthcare research.
Your Required Profile:
- Bachelor’s degree in Statistics, Mathematics, Computer Science, Biostatistics, Epidemiology, or a closely related quantitative field.
- Foundational knowledge of statistical programming. Academic coursework, projects, or internship experience using SAS or R is required.
- Strong analytical and problem-solving skills with exceptional attention to detail.
- A willingness to learn and a proactive approach to professional development.
- Ability to work collaboratively in a team environment and communicate effectively.
- Basic familiarity with clinical research or data management processes is advantageous, but not required.
What Will Make You Stand Out:
- A demonstrated interest in the pharmaceutical or healthcare industry.
- Exposure to CDISC standards through coursework or projects.
- Strong academic performance and a passion for data science.
Why Start Your Programming Career at ICON?
1. World-Class Training & Structured Mentorship
- Receive comprehensive, on-the-job training in SAS programming, CDISC standards, and clinical trial processes.
- Benefit from a formal mentoring program and a supportive team environment dedicated to your growth.
- This role is the recognized first step on the ICON career ladder to Statistical Programmer II, Senior Programmer, and Lead roles.
2. Purpose-Driven Work from Day One
- Your programming contributes directly to the analysis of clinical trials, impacting drug development and patient health.
- Gain exposure to a wide variety of therapeutic areas and study phases.
3. Comprehensive Benefits for Early Career Professionals
- Competitive entry-level salary and benefits package.
- Generous annual leave entitlements.
- Comprehensive health, life, and retirement benefits.
- Global Employee Assistance Programme and a culture that values inclusion, innovation, and professional growth.
Join a Culture that Invests in New Talent
At ICON, we believe that investing in the next generation of talent is crucial to shaping the future of clinical development. We are committed to creating an inclusive, accessible environment and encourage all qualified graduates to apply.
Ready to turn data into discovery and begin your journey as a statistical programmer?
If you have a quantitative degree and foundational programming skills, apply now to launch your career at ICON.
