Senior Analytical Data Programmer – Clinical Trials

Roche; Welwyn; On-site; GBP 65,000 - 90,000; Full time

Job summary

Roche is seeking an Analytical Data Science Programmer to transform statistical analysis plans into high-quality programming deliverables, including SDTM/ADaM datasets and tables, listings, and figures. You will develop datasets, validate outputs, and generate interactive dashboards for regulatory submissions and insights.

Work spans exploratory analyses, cross-functional collaboration, and scalable analytics across clinical programs in a modern, insight-driven environment.

Qualifications

• Bachelor's or Master's degree in Statistics, CS, Mathematics, Life Sciences, or related field.
• Solid experience in statistical programming in a clinical development setting.
• Proficient in SAS or R and visualization/review tools.
• Strong understanding of CDISC standards (SDTM/ADaM).
• Ability to deliver programming outputs independently.
• Fluent in English.

Responsibilities

• Develop, validate, and maintain SDTM/ADaM datasets and tables, listings, and figures (TLFs).
• Create interactive dashboards and data visualizations for regulatory and scientific use.
• Collaborate with cross-functional teams across biostatistics, data management and clinical operations.
• Translate analysis plans into executable programming specifications to ensure rigor.
• Ensure regulatory compliance and maintain audit trails for study files.
• Provide programming leadership for assigned studies and coordinate deliverables.

Skills

Statistical programming

SDTM/ADaM knowledge

Independent delivery

English fluency

Education

Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field

Tools

SAS

R

Visualization tools

Job description

Roche is seeking an Analytical Data Science Programmer to transform statistical analysis plans into high-quality programming deliverables, including SDTM/ADaM datasets and tables, listings, and figures. You will develop datasets, validate outputs, and generate interactive dashboards for regulatory submissions and insights.

Work spans exploratory analyses, cross-functional collaboration, and scalable analytics across clinical programs in a modern, insight-driven environment.