Senior/Principal Statistical Programmer Consultant - Remote

Overview

As a Senior/Principal Statistical Programmer Consultant, you will work directly for a single sponsor while enjoying the security and career opportunities that a global CRO provides. This role requires confidence and the ability to work independently while establishing trust with clients.

In Short

• Participate in CRF design and data management plans.
• Produce data listings, summary tables, and graphics for analyses.
• Integrate data across studies and validate programs.
• Coordinate data transfer with CROs and vendors.
• Collaborate with Biometrics functions for clinical trial data analysis.
• Handle ad-hoc requests and create presentations.

Requirements

• 10+ years of SAS programming experience in the pharmaceutical industry.
• Expertise in SAS programming language and validation standards.
• Experience with CDISC data standards.
• Prior experience in an FDA-regulated environment.
• Ability to manage multiple tasks and meet deadlines.

Benefits

• Work with a global CRO focused on quality and professional development.
• Opportunity to work directly with clients.
• Supportive work culture.