Principal Statistical Programmer (SAS+R) - Remote

Farmatalent; País Vasco; Remote; EUR 70,000 - 100,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to be fully embedded with a pharmaceutical client, delivering SDTM/ADaM specifications and complex analyses, with SAS and R expertise.

You will oversee CRO programmers, ensure regulatory deliverables, and contribute to study reports and submissions, while maintaining compliance with GCP, FDA/ICH guidelines.

This remote role offers autonomy and opportunities to drive quality in global clinical development programs.

Qualifications

• Bachelor's degree in CS/DS/Math/Statistics required.
• 7+ years as a Statistical Programmer in biotech/pharma clinical development.
• Expert SAS programming and CDISC SDTM/ADaM, Define.xml experience.
• Experience with regulatory submissions and FDA/ICH guidelines.
• Ability to work independently and lead CRO programming efforts.

Responsibilities

• Generate SDTM/ADaM datasets and define.xml for multiple studies.
• Develop SAS programs for tables, listings, and graphs.
• Oversee CRO programmers and ensure on-time delivery.
• Support study reports, regulatory submissions, and DSURs.

Skills

SAS programming

R programming

CDISC SDTM/ADaM

Define.xml

GxP FDA/ICH

Clinical programming leadership

Data analysis & statistics

Communication skills

Independence

Education

Bachelor's degree in Computer Science / Data Science / Mathematics / Statistics

Tools

SAS

R

Python

Unix/Linux

Job description

Cytel is seeking a Senior/Principal Statistical Programmer to be fully embedded with a pharmaceutical client, delivering SDTM/ADaM specifications and complex analyses, with SAS and R expertise.

You will oversee CRO programmers, ensure regulatory deliverables, and contribute to study reports and submissions, while maintaining compliance with GCP, FDA/ICH guidelines.

This remote role offers autonomy and opportunities to drive quality in global clinical development programs.