Junior Statistical Programmer - Clinical Trials (SAS)

Cytel; Tallahassee (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

Cytel invites a Recent Graduate to join as a Statistical Programmer, supporting data manipulation, analysis and reporting for Phase I–IV trials. You will work within a sponsor-dedicated program, backed by Cytel, on one pharmaceutical client driving next-generation treatments.

The role emphasizes SAS programming, dataset and TLF creation, ad-hoc reporting, and submission preparation, with opportunities to grow in a globally dispersed team and learn Cytel's standard processes.

Qualifications

• Minimum of 4 years of Undergraduate study plus 2 years of Graduate-level education.
• Academic training in Statistics, Epidemiology, or Data Science.
• Academic training in Computer Science, Mathematics, or Computational Science.
• Foundational data manipulation, analysis and reporting skills.
• Familiarity with drug development lifecycle and a passion to learn.
• Ability to work effectively in a globally dispersed team with cross-cultural partners.
• Excellent oral and written English communication skills.
• Ability to provide quality output and deliverables within challenging timelines.
• Willingness to learn and follow Cytel's standard processes.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data using SAS.
• Create and validate datasets/analysis files, tables, listings, and figures (TLFs).
• Generate ad-hoc reports to support trials.
• Prepare and validate submission packages.
• Apply understanding/experience with efficacy analysis.
• Collaborate effectively with team to meet deadlines.
• Adapt to changing priorities and processes.

Skills

SAS programming

Clinical data analysis

Team collaboration

English communication

Data manipulation

Education

Statistics, Epidemiology, or Data Science

Computer Science, Mathematics, or Computational Science

Tools

SAS

Job description

Cytel invites a Recent Graduate to join as a Statistical Programmer, supporting data manipulation, analysis and reporting for Phase I–IV trials. You will work within a sponsor-dedicated program, backed by Cytel, on one pharmaceutical client driving next-generation treatments.

The role emphasizes SAS programming, dataset and TLF creation, ad-hoc reporting, and submission preparation, with opportunities to grow in a globally dispersed team and learn Cytel's standard processes.