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 Biotechnology or Pharmaceutical industry.

Locations

• United States

Requirements

• Bachelor's degree required
• 8+ years SAS programming experience
• Knowledge of ICH guidelines and CDISC data structures

Responsibilities

• Support and lead SAS programming efforts
• Generate SDTM and ADaM datasets
• Perform quality control for SAS programs
• Interact with clients and lead programming efforts
• Prepare reports for Data Monitoring Committees
• Assist with training of new hires
• Program and document global utility programs
• Lead cross-functional development activities

Benefits

• Health insurance
• Retirement savings
• Life insurance
• Disability benefits
• Parental leave
• Paid time off
• Discretionary annual bonus