Sr Statistical Programming Specialist (R Programming)

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

• 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 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

• Strong analytical and problem-solving skills

• Excellent communication and ability to work in a team environment

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

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