Statistical Programmer III/IV

Job Summary

Providing statistical programming expertise, the full-time Statistical Programmer III/IV will coordinate with statisticians to develop and maintain efficient code for data analysis and reporting, with the option to work fully remotely.

Key responsibilities

• Gather and document requirements for developing or modifying existing programs and systems
• Generate, document, and maintain analysis datasets while creating various reports for clinical trials
• Collaborate with cross-functional teams to resolve data quality and analysis issues, contributing to mentoring junior programmers

Required qualifications

• Bachelor's degree in Public Health, Statistics, Computer Science, or a related field
• 4-5 years of experience as a SAS or R programmer in a clinical trials or health research setting
• Advanced programming skills in SAS or R, including experience with reporting and macro/package development
• Knowledge of clinical trials research data and biostatistics
• Ability to use Perl or other scripting languages for data manipulation and automation tasks