Principal Statistical Programmer

A company is looking for a Principal Statistical Programmer FSP.

Key Responsibilities

Provide technical leadership in SAS programming for clinical trial data analysis and reporting

Create, review, and approve documentation for data analysis and submissions

Ensure compliance with regulations and perform quality control checks on SAS code

Qualifications

MS in biostatistics or a related field with 8+ years of experience, or BS with 10+ years of experience in the pharmaceutical industry

Proven expertise in SAS language and procedures used in clinical trial reporting

R programming experience is a plus

Ability to interact across multiple functions with adaptability to changing priorities