As a Senior Statistical Programmer, you will apply advanced SAS programming and CDISC SDTM/ADaM expertise to support or lead clinical trials across phases. You will work embedded with a global pharmaceutical client, with remote work options, contributing to data analysis, reporting, and submission readiness. Your role focuses on generating datasets, TLFs, and submission documents while collaborating with cross-functional teams. This position offers growth within a values-driven environment that emphasizes scientific rigor and innovation.
Pay / Benefits
fully remote work option
training and development support
collaboration with global teams
opportunity to work with a sponsor and Cytel backing
competitive exposure to pharma biotech industry
growth opportunities within a senior role
Responsibilities
Manipulate, analyze, and report clinical trial data (safety and efficacy) using SAS
Create and validate SDTM/ADaM datasets and analysis files, as well as tables, listings, and figures
Produce and QC validation programming and complex ad-hoc reports
Apply Efficacy analysis expertise to projects
Assist in creating and reviewing submission documents and eCRTs
Communicate with internal teams and the client to clarify specifications and issues
Take lead duties when required
Collaborate effectively in a globally dispersed, cross-cultural team environment
Key requirements
8+ years SAS programming experience with clinical trial data in pharma/biotech (bachelor's degree)
6+ years experience with a master's degree or higher
Strong SAS data manipulation, analysis, and reporting skills
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