Senior Statistical Programmer R

As an ideal candidate for this role, you should have a Bachelor's degree in a quantitative field such as Statistics, Mathematics, Computer Science, or Data Science. Additionally, you should possess a minimum of 3 years of experience in R programming, including familiarity with R packages like Tidyverse, ggplot2, and survival. It is essential that you are well-versed in data visualization techniques and tools in R and have experience with clinical trial data, along with knowledge of CDISC ADaM and SDTM standards. Familiarity with Industry R packages like ADMIRAL and OAK is also desirable. Your solid analytical and problem-solving skills, paired with excellent communication and teamwork abilities, will be crucial in this role.

In this position, your primary responsibilities will include:

• Developing and maintaining the global R codebase for generating CDISC ADaM datasets and tables, listings, and figures in alignment with clinical trial data requirements.
• Ensuring compliance with industry standards and regulatory requirements.
• Collaborating with cross-functional teams to comprehend and implement project-specific data needs.
• Providing technical expertise and support for data analysis and reporting tasks.
• Performing quality control and validation of outputs to guarantee accuracy and consistency.
• Contributing to process improvements and the development of programming standards using R.

If you meet the qualifications and are excited about contributing to a dynamic team, we encourage you to apply for this opportunity. As an ideal candidate for this role, you should have a Bachelor's degree in a quantitative field such as Statistics, Mathematics, Computer Science, or Data Science. Additionally, you should possess a minimum of 3 years of experience in R programming, including familiarity with R packages like Tidyverse, ggplot2, and survival. It is essential that you are well-versed in data visualization techniques and tools in R and have experience with clinical trial data, along with knowledge of CDISC ADaM and SDTM standards. Familiarity with Industry R packages like ADMIRAL and OAK is also desirable. Your solid analytical and problem-solving skills, paired with excellent communication and teamwork abilities, will be crucial in this role.

In this position, your primary responsibilities will include:

• Developing and maintaining the global R codebase for generating CDISC ADaM datasets and tables, listings, and figures in alignment with clinical trial data requirements.
• Ensuring compliance with industry standards and regulatory requirements.
• Collaborating with cross-functional teams to comprehend and implement project-specific data needs.
• Providing technical expertise and support for data analysis and reporting tasks.
• Performing quality control and validation of outputs to guarantee accuracy and consistency.
• Contributing to process improvements and the development of programming standards using R.

If you meet the qualifications and are excited about contributing to a dynamic team, we encourage you to apply for this opportunity.