01Overview
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 .
