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As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in 100 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Key Responsibilities Develop and maintain R programs for generating CDISC SDTM and ADaM datasets and tables, listings, and figures in accordance with clinical trial data requirements Ensure compliance with industry standards and regulatory requirements Collaborate with cross-functional teams to understand and implement project-specific data needs Provide technical expertise and support for data analysis and reporting tasks Perform quality control and validation of outputs to ensure accuracy and consistency Qualifications Bachelors degree in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Data Science) Minimum of 3 years of experience in R programming including familiarity with R packages used in the analysis and reporting of data for clinical trials Familiarity with data visualization techniques and tools in R Experience with clinical trial data and familiarity with CDISC ADaM and SDTM standards Solid analytical and problem-solving skills Excellent communication and ability to work in a team setting Desirable Skills Knowledge of other open-source packages and tools Experience with SAS software Familiarity with CRAN, POSIT, and other open-source repositories and products .