Transform clinical data into life-changing insights. ICON is seeking an experienced Statistical Programmer II to develop and validate complex statistical programs for clinical trial analysis. In this key role, you will use your expertise in SAS or R to ensure the accuracy and integrity of clinical data, directly contributing to the interpretation of study results and the successful delivery of global research projects.
Key Responsibilities
You will be a senior technical contributor, responsible for the programming and validation of statistical outputs that support regulatory submissions.
Statistical Programming & Analysis:
- Develop, validate, and maintain complex statistical programs using SAS, R, or Python for data manipulation, analysis, and reporting of clinical trial data.
- Prepare and review key documents, including Statistical Analysis Plans (SAPs), programming specifications, and derived datasets (SDTM, ADaM).
- Ensure all programming outputs meet regulatory submission standards and comply with ICH/GCP guidelines.
Collaboration & Mentorship:
- Collaborate closely with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical methodologies.
- Mentor junior programmers, providing guidance on programming techniques, validation practices, and industry best practices.
- Effectively communicate complex statistical concepts and results to non-technical stakeholders.
Your Profile
Essential Qualifications:
- Bachelor’s degree in Statistics, Mathematics, Computer Science, or a related field.
- 5+ years of experience as a Statistical Programmer within the pharmaceutical, biotechnology, or CRO industry.
- Strong proficiency in SAS (primary) or R/Python for clinical data analysis.
- In-depth knowledge of CDISC standards (SDTM/ADaM) and statistical methodologies.
Required Skills:
- Strong analytical and problem-solving skills with meticulous attention to detail.
- Excellent communication and collaboration skills for effective teamwork.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
Preferred Qualifications:
- Advanced degree (Master's) in a relevant field.
Why Join ICON?
Our success depends on our people. When you join ICON, you become part of a team dedicated to excellence in clinical development. We offer:
- Competitive salary and a comprehensive benefits package focused on well-being.
- Health insurance and competitive retirement planning.
- Global Employee Assistance Programme and extensive well-being support.
- A diverse, inclusive culture that rewards high performance and nurtures talent.
Ready to shape the future of clinical development? We encourage you to apply even if you don't meet every single requirement. Your unique experience is valuable to us.
