Senior Statistical Programmer

Overview

Key member of Biostatistics team providing data analyses for clinical drug development.

Ideal candidate should have 3+ years of SAS programming experience and knowledge of CDISC standards.

Locations

• United Kingdom, England, London

Requirements

• 3+ years of clinical trial SAS programming experience
• Knowledge of CDISC standards
• BSc or higher in mathematics, statistics, computer science or related discipline

Responsibilities

• Perform programming activities across multiple studies
• Write SAS programs for datasets and outputs
• Adhere to CDISC standards
• Deliver outputs to agreed timelines
• Participate in design/review of programming deliverables
• Oversee outsourced statistical programming tasks