Senior Clinical Trials Statistical Programming Engineer

Quick Facts

• Senior Clinical Trials Statistical Programming Engineer (R/SAS)
• Remote work

Description

Support statistical programming activities across the clinical trial reporting process, from Statistical Analysis Plan (SAP) to Clinical Study Report (CSR) and regulatory submissions. Develop and maintain R-based solutions for clinical trial data processing, and prepare and optimize TLFs (Tables, Listings, and Figures). Collaborate with statisticians, programmers, and business stakeholders in an Agile/Kanban delivery environment.

Responsibilities

• Support statistical programming across the clinical trial reporting process (SAP to CSR/regulatory submissions)
• Develop and maintain R-based solutions for clinical trial data processing
• Prepare and optimize TLFs (Tables, Listings, Figures)
• Collaborate with statisticians, programmers, and business stakeholders
• Deliver work within an Agile/Kanban environment

Requirements

• Strong experience in Clinical Trials Statistical Programming
• Solid understanding of the process from SAP to CSR and submission deliverables
• Strong R programming skills
• Working knowledge of SAS
• Excellent communication skills and fluent English

Benefits

• Ongoing support from a dedicated agent for project continuity, client contact, and necessary formalities
• Consultant Development Program with growth planning and mentorship
• Access to 7N Learning & Development (webinars, article library, industry reports, development events)
• Integration events (e.g., annual Kick-Off trip, Christmas parties, sports events)
• Professional development and knowledge transfer opportunities
• Complete benefits package, including funding for medical care, life insurance, sports cards, and discounts in Poland and abroad