{"id":4000430,"url":"https://alion.io/job/icon-principal-statistical-programmer-5","title":"Principal Statistical Programmer","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":85,"open_postings":57,"ghost_share":0,"stale_share":0.772,"repost_share":0.018,"time_to_fill_p50_days":19,"computed_at":"2026-11-09T06:03:00Z"}},"role":"Sales","role_family":"Sales","seniority":"lead","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Bucharest, Romania","Warsaw, Poland","Budapest, Hungary","Sofia, Bulgaria","Johannesburg, South Africa","Kenya"],"countries":["RO","PL","HU","BG","ZA","KE"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CDISC","optional":false}],"status":"live","first_seen_at":"2026-11-09T00:00:00Z","employer_posted_date":"2026-11-09","last_verified_at":"2026-11-10T03:13:57Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Principal Statistical ProgrammerAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nWe are currently seeking a Principal Statistical Programmer to join our diverse and dynamic team. As a Principal 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.\nWhat You Will Be Doing:\nDeveloping and validating R programs for statistical analysis and reporting of clinical trial data.\nLeading 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.\nCollaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.\nPerforming quality control and validation of statistical outputs, ensuring accuracy, consistency, and regulatory compliance.\nAssisting in the preparation of statistical reports, presentations, and publications to support regulatory submissions and clinical study reporting.\nContributing to process improvements by identifying efficiencies in programming practices, automation, and the use of R-based analytical workflows.\nSupporting the development, maintenance, and enhancement of standardized R programming tools, macros, and reporting solutions across studies.\nYour Profile:\nBachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related quantitative field.\n8+ years' experience in statistical programming within a clinical research, biotechnology, or pharmaceutical environment.\nStrong exposure to leading programming activities for clinical studies. \nStrong proficiency in R programming, including the development and validation of clinical trial datasets, analyses, and reporting outputs.\nGood understanding of CDISC standards, including SDTM and ADaM, and their application within clinical trials.\nFamiliarity with regulatory requirements and industry guidance related to statistical programming and clinical data reporting.\nExcellent analytical and problem-solving skills, with a keen attention to detail.\nStrong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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