01Overview
Job descriptionAs 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 requirementsEnsure compliance with industry standards and regulatory requirementsCollaborate with cross-functional teams to understand and implement project-specific data needsProvide technical expertise and support for data analysis and reporting tasksPerform quality control and validation of outputs to ensure accuracy and consistencyQualifications
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 trialsFamiliarity with data visualization techniques and tools in RExperience with clinical trial data and familiarity with CDISC ADaM and SDTM standardsStrong analytical and problem-solving skillsExcellent communication and ability to work in a team environmentDesirable Skills
Knowledge of other open-source packages and toolsExperience with SAS softwareFamiliarity with CRAN, POSIT, and other open-source repositories and products
