Principal Statistical Programmer (SAS + R) - Remote

Eaton Corporation; Meira; Remote; EUR 60,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role, embedded with a pharmaceutical client. You will lead SAS and R programming for clinical trials, develop SDTM/ADaM outputs, and review complex datasets with minimal supervision.

You will oversee CRO deliverables, support regulatory submissions and reports, and ensure compliance with FDA and GCP standards across multiple studies.

Qualifications

• Extensive experience in SAS programming for clinical trials.
• Experience with SDTM/ADaM datasets and automated reporting.
• Knowledge of FDA regulations and GCP guidelines.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml for multiple studies.
• Develop SAS programs to generate datasets, listings, tables and graphs for clinical trials.
• Deliver high-quality statistical programming results using SAS and R as needed.

Skills

SAS

R

Clinical programming

Regulatory compliance

CRO coordination

Tools

define.xml

ADaM

SDTM

Job description

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role, embedded with a pharmaceutical client. You will lead SAS and R programming for clinical trials, develop SDTM/ADaM outputs, and review complex datasets with minimal supervision.

You will oversee CRO deliverables, support regulatory submissions and reports, and ensure compliance with FDA and GCP standards across multiple studies.