Senior Statistical Programmer Consultant

A company is looking for a Senior Statistical Programmer Consultant to join a client-focused team.

Key Responsibilities

Perform end-to-end SAS programming for Phase III clinical trials

Develop and validate SDTM, ADaM datasets, and TLFs in compliance with CDISC standards

Support BLA submissions, including regulatory-ready deliverables

Required Qualifications

Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field

7+ years of experience in statistical programming within the pharmaceutical or CRO environment

Experience supporting Phase III studies and BLA submissions

Advanced proficiency in SAS programming, including macro development

Solid understanding of CDISC standards (SDTM, ADaM)