Clinical SAS Programmer — Embedded in Global Pharma Program

Cytel; Pennsylvania; On-site; USD 70,000 - 90,000; Full time

Job summary

Cytel seeks a recent graduate Statistical Programmer to join our embedded client program, performing SAS-driven data manipulation, analysis, and reporting for Phase I–IV trials. You will develop skills alongside Cytel and a trusted pharmaceutical partner, handling datasets, tables, listings, and figures with the opportunity to contribute to submission-ready packages.

You’ll work in a globally dispersed team, applying foundational data skills and learning our standard processes while delivering

Qualifications

• A minimum of 4 years of Undergraduate study and 2 additional years of Graduate-level education.
• Academic training in Statistics, Epidemiology, or Data Science and in Computer Science, Mathematics, or Computational Science.
• Foundational data manipulation, analysis and reporting skills.
• Familiarity with drug development life cycle and a passion to learn.
• Ability to work effectively in a globally dispersed team with cross-cultural partners.
• Excellent English communication skills and ability to deliver under deadlines.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data, including safety and efficacy, using SAS programming.
• Create and validate datasets/analysis files, tables, listings, and figures (TLFs).
• Generate ad-hoc reports.
• Prepare and validate submission packages.
• Apply understanding/experience with efficacy analysis.
• Work as a team member, meeting deadlines and adapting to priorities.

Skills

SAS programming

Data manipulation

Ad hoc reporting

Team collaboration

Education

Undergraduate + Graduate education

Statistics, Epidemiology, or Data Science

Computer Science, Mathematics, or Computational Science

Tools

SAS

Job description

Cytel seeks a recent graduate Statistical Programmer to join our embedded client program, performing SAS-driven data manipulation, analysis, and reporting for Phase I–IV trials. You will develop skills alongside Cytel and a trusted pharmaceutical partner, handling datasets, tables, listings, and figures with the opportunity to contribute to submission-ready packages.

You’ll work in a globally dispersed team, applying foundational data skills and learning our standard processes while delivering