Senior Statistical Programmer

Senior Statistical Programmer - RICON 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 Senior Statistical Programmer to join our diverse and dynamic team. As a Senior Statistical Programmer at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs in R, collaborating with biostatisticians, and ensuring compliance with regulatory standards.What You Will Be Doing:Developing and validating R programs for statistical analysis and reporting of clinical trial data.Leading more than one Statistical Programming team to create, validate and generate statistical outputs, including listings, tables, figures, and CDISC-compliant SDTM and ADaM datasets (including mapping specifications) of low to moderate complexity.Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.Performing quality control and validation of statistical outputs, ensuring accuracy, consistency, and regulatory compliance.Assisting in the preparation of statistical reports, presentations, and publications to support regulatory submissions and clinical study reporting.Contributing to process improvements by identifying efficiencies in programming practices, automation, and the use of R-based analytical workflows.Supporting the development, maintenance, and enhancement of standardized R programming tools, macros, and reporting solutions across studies.Your Profile:Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related quantitative field.Experience in statistical programming within a clinical research, biotechnology, or pharmaceutical environment.Strong proficiency in R programming, including the development and validation of clinical trial datasets, analyses, and reporting outputs.Good understanding of CDISC standards, including SDTM and ADaM, and their application within clinical trials.Familiarity with regulatory requirements and industry guidance related to statistical programming and clinical data reporting.Excellent analytical and problem-solving skills, with a keen attention to detail.Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.Employment 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 incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Visit our careers site to read more about the benefits ICON offers.Inclusion and AccessibilityICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.Are you a current ICON Employee? Please click here to applySummaryLocation: Poland, Warsaw; France, Paris; Spain, Madrid; Hungary, Budapest; UK, Reading; Germany, Frankfurt; Belgium, Mechelen; Italy, Milan; South Africa, Johannesburg; Ireland, DublinType: Full time