Principal Statistical Programmer (SAS + R) — Remote

National Association Of Consumer Bankruptcy Attorneys; Madrid; Remote; EUR 116,000 - 152,000; Full time

Job summary

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to lead statistical programming for clinical development programs. You will implement reporting and analysis activities, supervise CRO programmers, and contribute to regulatory submissions with strong SAS and R expertise.

The role demands independence, deep knowledge of CDISC standards, and proven ability to deliver high-quality results across therapeutic areas. Collaboration with sponsors and FDA-facing teams is essential.

Qualifications

• Bachelor's degree in computer science, data science, mathematics, or statistics.
• 7+ years of experience as a Statistical Programmer in Biotech/Pharma clinical development.
• Exceptional SAS programming skills in a clinical development environment.
• Extensive experience with CDISC standards (SDTM, ADaM, Define.xml).
• Experience supporting regulatory submissions and interactions with FDA/regulators.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guides and Define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables and complex graphs.
• Deliver high-quality SAS/R programming results for clinical development programs.
• Oversee CRO programming deliverables to ensure quality and timelines.
• Support preparation of clinical study reports, regulatory submissions, DSURs and exploratory analyses.

Skills

SAS programming

R programming

CDISC SDTM

CDISC ADaM

FDA/ICH regulation

Regulatory submissions

Education

Bachelor's degree in CS/Data Science/Math/Statistics

Tools

SAS

R

Unix/Linux

Git

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to lead statistical programming for clinical development programs. You will implement reporting and analysis activities, supervise CRO programmers, and contribute to regulatory submissions with strong SAS and R expertise.

The role demands independence, deep knowledge of CDISC standards, and proven ability to deliver high-quality results across therapeutic areas. Collaboration with sponsors and FDA-facing teams is essential.