Principal Statistical Programmer (Remote) – SAS & R

Jobgether; Santiago de Compostela; Remote; EUR 70,000 - 110,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role with one global pharmaceutical client. You will lead SAS and R programming for clinical studies, generate SDTM/ADaM outputs, and oversee CRO deliverables while ensuring regulatory compliance.

You will work with FDA guidelines, contribute to study reports, and develop standards for programming tools across multiple trials. This role emphasizes autonomy and ownership within a sponsor-driven environment.

Responsibilities

• Generate SDTM, ADaM specs, datasets, reviewer’s guide and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality SAS and/or R programming outputs for clinical programs.
• Oversee CRO programmers to ensure quality and timely delivery.
• Support preparation of study reports, regulatory submissions, DSURs and explorations.
• Apply FDA regulations governing reporting of trial data and GCP guidelines.
• Contribute to standards for programming tools, outputs, and macros.
• Contribute to CRFs, edit checks, and data validation plans.
• Review and/or author data transfer specifications for external data.
• Collaborate with CROs, vendors, and partners to meet timelines.

Skills

SAS

R

Clinical trials

SDTM/ADaM

Regulatory knowledge

Job description

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role with one global pharmaceutical client. You will lead SAS and R programming for clinical studies, generate SDTM/ADaM outputs, and oversee CRO deliverables while ensuring regulatory compliance.

You will work with FDA guidelines, contribute to study reports, and develop standards for programming tools across multiple trials. This role emphasizes autonomy and ownership within a sponsor-driven environment.