Senior Statistical Programmer

Senior Statistical Programmer - Client BasedICON 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’re looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward?thinking team.At ICON, you’ll play an integral role in transforming clinical trial data into meaningful insights that drive critical decision?making in global healthcare.In this role, you’ll take ownership of developing and validating high?quality statistical programs, partnering closely with expert biostatisticians, and ensuring our outputs meet the highest scientific and regulatory standards.Your expertise will directly support the success of our clinical studies and the advancement of life?changing therapies.What You Will Be DoingDesigning, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.Supporting the creation of statistical reports, presentations, and regulatory submission documentation.Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.Your ProfileBachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related discipline.Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.Exceptional analytical and problem?solving abilities, with meticulous attention to detail.Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.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: South Africa, Johannesburg; Spain, Madrid; Bulgaria, Sofia; Romania, Bucharest; Portugal, Lisbon; Estonia, Tallinn; Poland, Warsaw; Ireland, Dublin; Spain, Barcelona; Croatia, Zagreb; Lithuania, Vilnius; Czech Republic, Prague; Poland, Gdansk; KenyaType: Full time

Your expertise will directly support the success of our clinical studies and the advancement of life?changing therapies.What You Will Be DoingDesigning, developing, and validating SAS programs to support statistical analysis and reporting of clinical trial data.Collaborating with biostatisticians to shape analysis plans, identify appropriate methodologies, and deliver reliable insights.Conducting comprehensive quality control checks to ensure the accuracy, consistency, and integrity of statistical outputs.Supporting the creation of statistical reports, presentations, and regulatory submission documentation.Identifying opportunities to enhance programming processes, contributing to continuous improvement and innovation within the team.Your ProfileBachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related discipline.Proven experience in statistical programming, ideally within clinical research or the pharmaceutical industry.Strong command of SAS programming, with a solid grounding in statistical concepts and clinical data analysis.Exceptional analytical and problem?solving abilities, with meticulous attention to detail.Effective communicator with strong teamwork skills and the confidence to translate complex analyses into clear, actionable insights.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

Senior Statistical Programmer - Client BasedICON 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’re looking for a talented Senior Statistical Programmer to become a key contributor within our diverse, collaborative, and forward?thinking team.