Statistical Programmer I: Shape Clinical Data & Reports

FTLEE Fortrea Clinical Research Unit Ltd; Leeds; On-site; GBP 32,000 - 52,000; Full time

Job summary

Fortrea Clinical Research Unit Ltd is seeking a Statistical Programmer 1 in Leeds to join a global team transforming trial data into high-quality datasets and reports. You will work with biostatisticians, data managers, and clinical teams to support regulatory submissions and critical drug development decisions.

You will develop, validate, and maintain SAS programs, create SDTM/ADaM datasets, and produce TFLs while ensuring CDISC standards and data integrity across studies.

Qualifications

• BSc in Statistics, Mathematics, Computer Science, Data Science, Life Sciences, or a related field.
• Strong analytical, problem-solving, and organizational skills.
• Attention to detail and ability to work with complex data.
• Effective communication and teamwork skills.
• Proficiency in MS Office, particularly Excel.
• Familiarity with SAS, R, Python, SQL, or similar tools.
• Knowledge of clinical research or healthcare data is advantageous.

Responsibilities

• Develop, validate, and maintain SAS programs for data analysis and reporting.
• Create and support SDTM and ADaM datasets.
• Produce Tables, Figures, and Listings (TFLs) for study reporting.
• Perform quality control and validation of programming outputs.
• Produce Define XML/PDFs, ARM, annotated CRFs and Reviews Guides to support SDTMs and ADaMs.
• Follow CDISC standards, regulatory requirements, and internal processes.
• Contribute to study deliverables across multiple therapeutic areas and development phases.

Skills

Analytical thinking

Attention to detail

Effective communication

Teamwork

Time management

Multitasking

Education

BSc in Statistics

Tools

SAS

R

Python

SQL

MS Excel

Job description

Fortrea Clinical Research Unit Ltd is seeking a Statistical Programmer 1 in Leeds to join a global team transforming trial data into high-quality datasets and reports. You will work with biostatisticians, data managers, and clinical teams to support regulatory submissions and critical drug development decisions.

You will develop, validate, and maintain SAS programs, create SDTM/ADaM datasets, and produce TFLs while ensuring CDISC standards and data integrity across studies.