Statistical Data Scientist

We are seeking a highly skilled programmer to support clinical trial data analysis and regulatory submissions.

Key Responsibilities :

• Author, validate and document programs applying good programming practices.
• Develop and maintain programs in R with hands-on experience in Tidyverse and Admiral packages.
• Create ADaM datasets using Admiral packages in R .
• Read and write raw data across SAS and R platforms .
• Conduct thorough debugging using R console tools .
• Review and approve clinical trial documents dataset specifications and TFL shells .
• Identify and resolve data issues outliers and standards-related discrepancies .
• Complete review and approve CDISC Validation Tool reports .
• Stay updated on emerging standards and assess impacts on ongoing and future trials .
• Maintain proficiency in SAS and awareness of developments in programming tools and standards .
• Ensure all study master file documents are audit-ready .
• Provide input into and review of project management documents .
• Perform all work in full compliance with applicable legislation regulations company policies and procedures .