Principal Statistical Programmer Consultant

Overview

Role involves statistical programming and data analysis in clinical trials.

Ideal candidate should have 10+ years of SAS programming experience in the pharmaceutical industry.

Locations

• United States

Requirements

• 10+ years SAS programming
• BA/BS in computer science/statistics/math or MA/MS with 8 years experience
• Expertise in SAS programming and validation standards
• Experience with CDISC data standards
• Experience in FDA-regulated environment
• Excellent verbal/written and interpersonal skills

Responsibilities

• Participate in CRF design and data management
• Produce data listings and summary tables
• Integrate data across studies
• Coordinate data transfer with CROs
• Collaborate with Biometrics functions
• Execute ad-hoc requests and presentations