ICON plcStatistical Programmer IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Statistical Programmer II to join our diverse and dynamic team. As a Statistical Programmer II at ICON, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis and real world evidence (RWE) studies. Your expertise will contribute to the accurate interpretation of clinical data, helping to ensure the successful delivery of research projects.
What You Will Be Doing:- Developing, validating, and maintaining complex statistical programs (primarily SAS, with R or Python as applicable) for data manipulation, analysis, and reporting across clinical trials and real world evidence studies.
- May help lead a Statistical Programming team to create, validate and generate statistical programs consisting of outputs such as listings, tables, figures, and SDTM/ADaM domains (including mapping specifications) of low to moderate complexity at a minimum.
- All programs must be developed in accordance with documented procedures and project-specific timelines to generate accurate, complete and consistent outputs.
- Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
- Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets, including SDTM and ADaM, to meet regulatory standards.
- Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
- Mentoring junior programmers and assisting in training team members on programming techniques and best practices.
Your Profile:- Bachelor's degree in statistics, mathematics, computer science, or a related field; advanced degree is a plus.
- Proven experience as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming, particularly SAS.
- Typically ≥ 3 years of experience.
- Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated.
- Strong experience working with SDTM/ADaM datasets and standards.
- Experience supporting real world evidence (RWE) studies is highly desirable.
- Proficiency in programming languages such as SAS, R, or Python, with experience in clinical data management systems.
- Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.
- Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.
#LI-SA1Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility: ICON is an equal opportunity employer committed to building an inclusive and accessible workplace. If you require reasonable accommodations during the recruitment process, please let us know. 
