Principal Statistical Programmer (SAS + R) – Remote

Grupo Noa’s; Comunidad Valenciana; Remote; EUR 65,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to work remote in Spain, dedicated to a sponsor client. The role focuses on leading programming activities across SDTM/ADaM, SAS and R, and oversight of CRO deliverables with strong regulatory awareness.

You will develop datasets, listings, and figures, contribute to study reports and regulatory submissions, and ensure data quality and standards across programs in a global setting.

Qualifications

• Senior statistical programmer with clinical development experience.
• Experience delivering SDTM/ADaM specifications and datasets.
• Familiar with FDA regulations and eCTD submissions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guide, and define.xml files.
• Develop SAS programs for datasets, tables, listings, and graphs.
• Deliver high-quality SAS and R programs for clinical development.
• Oversee CRO programming deliverables for multiple studies.
• Support clinical study reports, regulatory submissions, DSUR, and exploratory analyses.
• Understand FDA regulations affecting reporting of trial data.
• Contribute to standards for programming tools and macros.
• Develop CRFs, edit checks, and data validation plans.
• Provide review.

Skills

SAS programming

R programming

SDTM

ADaM

CRO oversight

FDA regulations

Clinical trials

Job description

Cytel is seeking a Senior/Principal Statistical Programmer to work remote in Spain, dedicated to a sponsor client. The role focuses on leading programming activities across SDTM/ADaM, SAS and R, and oversight of CRO deliverables with strong regulatory awareness.

You will develop datasets, listings, and figures, contribute to study reports and regulatory submissions, and ensure data quality and standards across programs in a global setting.