Remote Principal Statistical Programmer (SAS + R)

Profile Software Services; Santiago de Compostela; Remote; EUR 65,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to work in a remote setup, embedded with a pharmaceutical client. You will independently develop SAS and R programs for SDTM/ADaM datasets, tables, and figures, while overseeing CRO programmers to ensure timely delivery of high-quality outputs.

You will contribute to the preparation of regulatory submissions and study reports, while following FDA guidelines and industry standards for clinical trial data management.

Qualifications

• Proven experience delivering SAS programs for clinical trials.
• Proficiency in R for statistical analysis in pharma projects.
• Strong knowledge of SDTM/ADaM data standards and data mapping.

Responsibilities

• Develop SAS programs to create datasets, tables, and graphs for trials.
• Coordinate with CROs to ensure timely, high-quality programming deliverables.
• Support clinical study reports, regulatory submissions, and exploratory analyses.

Skills

SAS programming

R programming

Clinical data standards (SDTM/ADaM)

Tools

SAS Software

R Software

Job description

Cytel is seeking a Senior/Principal Statistical Programmer to work in a remote setup, embedded with a pharmaceutical client. You will independently develop SAS and R programs for SDTM/ADaM datasets, tables, and figures, while overseeing CRO programmers to ensure timely delivery of high-quality outputs.

You will contribute to the preparation of regulatory submissions and study reports, while following FDA guidelines and industry standards for clinical trial data management.