Principal Statistical Programmer

Overview

Role involves leading SAS programming efforts for clinical trials and providing technical expertise.

Ideal candidate should have 8+ years of SAS programming experience in the Biotech or clinical trials industry.

Locations

• Canada

Requirements

• Bachelor's degree in Statistics or related field
• 8+ years SAS programming experience
• Knowledge of ICH guidelines and CDISC data structures

Responsibilities

• Lead statistical programming efforts
• Generate SDTM and ADaM datasets
• Provide programming support for analyses
• Perform quality control for SAS programs
• Prepare reports for Data Monitoring Committees
• Assist with training of new hires
• Interact with clients
• Oversee generation of study documents