R & Clinical SAS programmer

Key Responsibilities

Develop and maintain global R codebase for generating CDISC 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
Contribute to process improvements and development of programming standards using R

Qualifications

Bachelor's 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 (e.g., Tidyverse, ggplot2, survival)
Familiarity with data visualization techniques and tools in R
Experience with clinical trial data and familiarity with CDISC ADaM and SDTM standards
Knowledge in Industry R packages like ADMIRAL and OAK
Strong analytical and problem-solving skills
Excellent communication and teamwork abilities

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