Sr. Statistical Programmer (Sponsor dedicated) - Experience in clinical trials working with SAS and R programming - Brazil Home Based

Role overview Lead statistical programming for clinical trial projects, turning analysis plans and specifications into reliable datasets, tables, listings, and graphs. The role combines hands-on programming and quality control with coordination of deliverables, project communication, and guidance for other programming staff. The position is home-based in Brazil and may involve occasional travel.

Responsibilities - Develop and validate programs that produce clinical trial outputs and derived datasets from statistical analysis plans and programming specifications. - Define dataset and output specifications, review study documents, and identify issues that could delay or complicate programming. - Check deliverables against quality standards, investigate discrepancies, and work with statisticians and project colleagues to resolve findings. - Lead programming activities, track progress, estimate timelines, and adapt workload across multiple projects. - Maintain complete, current documentation and verification records in line with procedures and relevant regulatory guidance. - Represent statistical programming in sponsor and project meetings, support team decisions, and mentor colleagues through training and feedback.

Requirements - Undergraduate degree, preferably in a scientific or statistical discipline, or an equivalent combination of education and demonstrated programming experience. - Extensive experience with SAS or other required programming software, preferably in clinical trials. - Strong written and verbal communication skills, including the ability to work effectively with cross-functional project teams. - Ability to read, write, speak, and understand English.

Benefits and work setup - Home-based role in Brazil with minimal travel potentially required.