Sr Statistical Programming Specialist

Role Overview: As a Data Scientist in the team, you will be responsible for developing and maintaining R programs to generate CDISC SDTM and ADaM datasets, as well as tables, listings, and figures to meet clinical trial data requirements. Key Responsibilities: - Ensuring compliance with industry standards and regulatory requirements - Collaborating with cross-functional teams to understand 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 maintain accuracy and consistency Qualification Required: - A Bachelor's degree in a quantitative field such as Statistics, Mathematics, Computer Science, or Data Science - At least 3 years of experience in R programming, including familiarity with R packages used in data analysis and reporting for clinical trials - Knowledge of data visualization techniques and tools in R - Experience working with clinical trial data and understanding of CDISC ADaM and SDTM standards - Strong analytical and problem-solving skills - Excellent communication skills and the ability to work effectively in a team environment Desirable skills that would be beneficial for this role: - Knowledge of other open-source packages and tools - Experience with SAS software - Familiarity with CRAN, POSIT, and other open-source repositories and products (Note: The company also provides more information about EEO & Accommodations request for your reference.),