Principal Statistical Programmer - SAS + R (Remote)

Deel; Murcia; Remote; EUR 90,000 - 120,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, embedded with a pharmaceutical client. You will take lead on SDTM/ADaM development, support CROs, and ensure compliant, high-quality programming for regulatory submissions.

The role requires 7+ years in Biotech/Pharma programming, strong SAS skills, CDISC expertise, and independent work capabilities. Collaboration with clinical teams across sites is essential.

Qualifications

• 7+ years of experience as a Statistical Programmer in Biotech/Pharma
• Exceptional SAS programming skills and experience in clinical development
• Experience with CDISC standards (SDTM, ADaM, Define.xml) and FDA/ICH regulation

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
• Develop SAS programs to create datasets, listings, tables, and graphs
• Deliver high-quality SAS and/or R programs for clinical development programs
• Oversee CRO programmers to ensure timely, compliant deliverables
• Support preparation of clinical study reports, regulatory submissions, and publications
• Ensure compliance with FDA regulations and good clinical practice

Skills

SAS programming

CDISC standards

Leadership

Education

Bachelor's degree in Computer Science, Data Science, Mathematics or Statistics

Tools

SAS

R

Unix/Linux

Git

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, embedded with a pharmaceutical client. You will take lead on SDTM/ADaM development, support CROs, and ensure compliant, high-quality programming for regulatory submissions.

The role requires 7+ years in Biotech/Pharma programming, strong SAS skills, CDISC expertise, and independent work capabilities. Collaboration with clinical teams across sites is essential.