Principal Statistical Programmer (SAS + R) - Remote

Manpower España; Barcelona; On-site; EUR 90,000 - 120,000; Full time

Job summary

Cytel seeks a Senior Principal Statistical Programmer to work on sponsor‑dedicated clinical development programs. You will implement reporting and analysis activities, generate SDTM/ADaM specifications, and oversee CRO programming deliverables with minimal supervision.

Responsibilities include creating datasets, tables, and graphs in SAS/R, supporting regulatory submissions, and contributing to programming standards. Location options include Madrid and Girona, Spain.

Qualifications

• Minimum a bachelor’s degree in CS/DS/Statistics or related field.
• 7+ years as Statistical Programmer in Biotech/Pharma Biostatistics or similar.
• Strong SAS programming and CDISC SDTM/ADaM experience.
• Experience supporting regulatory submissions and FDA/ICH guidance.
• Ability to work independently and lead CRO programming efforts.

Responsibilities

• Generate SDTM, ADaM specs, datasets, define.xml for studies.
• Develop SAS programs for datasets, tables, listings and graphs.
• Deliver high‑quality programming results for regulatory submissions.
• Oversee CRO programmers to meet timelines and quality.
• Support study reports, DSURs, publications, and exploratory analyses.
• Contribute to standards for programming tools and macros.

Skills

SAS programming

Statistical programming

CDISC standards

Independent work

Leadership

Education

Bachelor's degree in CS/DS/Statistics

Tools

SAS

R

Python

Job description

Cytel seeks a Senior Principal Statistical Programmer to work on sponsor‑dedicated clinical development programs. You will implement reporting and analysis activities, generate SDTM/ADaM specifications, and oversee CRO programming deliverables with minimal supervision.

Responsibilities include creating datasets, tables, and graphs in SAS/R, supporting regulatory submissions, and contributing to programming standards. Location options include Madrid and Girona, Spain.