Senior Principal Statistical Programmer (SAS/R) – Remote

Confiarte; Segovia; Remote; EUR 75,000 - 120,000; Full time

Job summary

Cytel is hiring a Senior/Principal Statistical Programmer (Remote) to work with a sponsor-dedicated pharmaceutical client. The role reports to Biostatistics and Programming leadership and entails independent program development and CRO oversight in a remote setting.

The successful candidate will implement reporting and analysis activities across multiple studies, ensure high-quality outputs, and align with FDA/GCP guidelines while contributing to standards and CRF/edit check development.

Qualifications

• Senior statistical programmer with extensive clinical trial experience.
• Expertise in SAS and R programming for datasets, listings and graphs.
• Knowledge of SDTM/ADaM standards and regulatory expectations.

Responsibilities

• Generate SDTM, ADaM specs, datasets, reviewer’s guide and define.xml for multiple studies.
• Develop SAS programs to produce datasets, complex listings, tables and graphs.
• Deliver high-quality programming results; validate and maintain SAS and R code.
• Oversee CRO programming deliverables to meet timelines.
• Support clinical study reports, regulatory submissions and DSUR analyses.
• Ensure compliance with FDA regulations and GCP guidelines.
• Help create standards for tools, outputs and macros.
• Assist in CRF development, edit checks, and data validation plans.
• Provide review and quality checks.

Skills

SAS programming

R programming

SDTM/ADaM specifications

CRO oversight

GCP/regulatory knowledge

Statistical programming leadership

Clinical trial data reporting

Tools

SAS

R

Job description

Cytel is hiring a Senior/Principal Statistical Programmer (Remote) to work with a sponsor-dedicated pharmaceutical client. The role reports to Biostatistics and Programming leadership and entails independent program development and CRO oversight in a remote setting.

The successful candidate will implement reporting and analysis activities across multiple studies, ensure high-quality outputs, and align with FDA/GCP guidelines while contributing to standards and CRF/edit check development.