Senior Principal Statistical Programmer — SAS + R (Remote)

Gft Technologies Se; Córdoba; Remote; EUR 70,000 - 110,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely on sponsor projects for a leading pharmaceutical client. The role emphasizes independent work, high-quality data analysis, and regulatory-compliant reporting across multiple studies.

You will develop SDTM/ADaM artifacts, write SAS and R code for complex listings and graphs, and supervise CRO programmers to ensure timely, high-quality outputs. Regulatory familiarity and adherence to GxP guidelines are required.

Qualifications

• Experience with SAS programming for clinical data and reports.
• Proficiency in R for statistical analyses and data visualization.
• Knowledge of CDISC SDTM/ADaM standards and regulatory expectations.

Responsibilities

• Generate SDTM/ADaM specifications, datasets, and define.xml files for studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality programming results and maintain SAS/R code for trials.
• Oversee CRO programmers to ensure timely, compliant deliverables.
• Support preparation of study reports, regulatory submissions, and analyses.
• Adhere to FDA/regulatory guidelines for electronic submissions.
• Contribute to standards for programming tools, outputs, and macros.
• Assist in CRF development, edit checks, and data validation plans.

Skills

SAS

R

SDTM

ADaM

Clinical standards

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely on sponsor projects for a leading pharmaceutical client. The role emphasizes independent work, high-quality data analysis, and regulatory-compliant reporting across multiple studies.

You will develop SDTM/ADaM artifacts, write SAS and R code for complex listings and graphs, and supervise CRO programmers to ensure timely, high-quality outputs. Regulatory familiarity and adherence to GxP guidelines are required.