Principal Statistical Programmer (SAS + R) — Remote

Nationale-Nederlanden; Brea de Aragón; Remote; EUR 60,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) for remote work with sponsor-dedicated engagement. The role focuses on delivering high-quality programming for clinical development, including SDTM/ADaM, datasets, listings, and defines.

You will oversee CRO deliverables and support study reports and regulatory submissions, while ensuring GCP compliance and standards across projects. The position requires extensive experience in SAS and R within clinical trials, data standards,

Qualifications

• Master's degree in Biostatistics or related field is required.
• Strong SAS and R programming experience in clinical trials.
• Experience with CDISC SDTM/ADaM and regulatory submissions.

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 statistical programming results including SAS and/or R programs
• Oversee CRO's statistical programming deliverables for multiple studies to meet timelines
• Support preparation of clinical study reports, regulatory submissions, publications
• Follow FDA regulations and GCP for electronic submissions
• Contribute to standards for programming tools and macros
• Develop CRFs, edit check specs, and data validation plans
• Provide review

Skills

SAS programming

R programming

CDISC SDTM/ADaM

Clinical trial data analysis

CRO oversight

GCP/regulatory awareness

Education

Master's degree in Biostatistics or related field

Tools

SAS

R

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) for remote work with sponsor-dedicated engagement. The role focuses on delivering high-quality programming for clinical development, including SDTM/ADaM, datasets, listings, and defines.

You will oversee CRO deliverables and support study reports and regulatory submissions, while ensuring GCP compliance and standards across projects. The position requires extensive experience in SAS and R within clinical trials, data standards,