Remote Senior/Principal Statistical Programmer (SAS + R)

Farmacias Trebol; Fuengirola; Remote; EUR 70,000 - 110,000; Full time

Job summary

Cytel Inc. is seeking a Principal Statistical Programmer to work remotely on sponsor-driven clinical development programs. You will design, implement, and validate SAS and R workflows, generate SDTM/ADaM datasets, tables, listings, and figures, and oversee CRO deliverables to ensure high quality and on-time submissions.

The role requires extensive CDISC experience, FDA/regulatory familiarity, and strong leadership and independence to drive projects across multiple therapeutic areas.

Qualifications

• Bachelor's degree in computer science, data science, mathematics, or statistics (preferred).
• 7+ years as Statistical Programmer in Biotech/Pharma Clinical Development Biometrics.
• Exceptional SAS programming and development of programming procedures.
• Extensive CDISC standards experience (SDTM, ADaM, Define.xml).
• Experience with regulatory submissions and working with FDA/global authorities.
• Ability to work independently; strong written and verbal communication; leadership skills.

Responsibilities

• Generate SDTM, ADaM specs, datasets, reviewer's guide and Define.xml for multiple studies.
• Develop SAS programs to produce datasets, listings, tables, and graphs; collaborate with statisticians.
• Deliver high-quality programming outputs; validate and maintain SAS/R programs for development programs.
• Oversee CROs' programming deliverables to meet timelines and quality.
• Support clinical study reports, regulatory submissions, publications, and DSURs.

Skills

SAS programming

Independent work

Communication

Leadership

Education

Bachelor's degree in computer science/data science/mathematics/statistics

Tools

SAS

R

Python

Git

Unix/Linux

Shiny

Job description

Cytel Inc. is seeking a Principal Statistical Programmer to work remotely on sponsor-driven clinical development programs. You will design, implement, and validate SAS and R workflows, generate SDTM/ADaM datasets, tables, listings, and figures, and oversee CRO deliverables to ensure high quality and on-time submissions.

The role requires extensive CDISC experience, FDA/regulatory familiarity, and strong leadership and independence to drive projects across multiple therapeutic areas.