Principal Statistical Programmer (SAS & R) – Remote Pharma

Epam Systems, Inc.; Barcelona; Remote; EUR 90,000 - 120,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role. You will work within sponsor projects, driving SAS and R programming for multiple clinical studies, and oversee CRO programmers to ensure high-quality data outputs.

You will contribute to SDTM/ADaM specifications, study reports, regulatory submissions, and exploratory analyses, while adhering to FDA guidelines and GCP standards.

Qualifications

• Senior-level statistical programming experience in clinical development.
• Familiar with FDA regulations, GCP, and electronic submissions.
• Experience overseeing CRO programmers and ensuring timely deliverables.

Responsibilities

• Generate SDTM and ADaM specifications, datasets, reviewer’s guides, and define.xml files.
• Develop SAS programs for datasets, listings, tables, and graphs with descriptive/inferential statistics.
• Deliver high-quality SAS and R programs tailored to clinical programs and support regulatory submissions.
• Oversee CRO programmers to ensure quality deliverables within timelines.
• Contribute to study reports, DSURs, publications, and data validation plans.

Skills

SAS programming

R programming

SDTM/ADaM

Clinical trial data

CRO supervision

Tools

SAS

R

Job description

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role. You will work within sponsor projects, driving SAS and R programming for multiple clinical studies, and oversee CRO programmers to ensure high-quality data outputs.

You will contribute to SDTM/ADaM specifications, study reports, regulatory submissions, and exploratory analyses, while adhering to FDA guidelines and GCP standards.