Principal Statistical Programmer (Remote) SAS & R

Auren; Las Palmas de Gran Canaria; Remote; EUR 70,000 - 95,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role. You will work on clinical development programs, implementing SDTM/ADaM specifications and generating complex datasets, tables, and figures in SAS and R.

You will also oversee CRO deliverables and contribute to regulatory submissions and exploratory analyses. The role requires senior-level expertise in statistical programming, with a focus on data standards, quality, and adherence to FDA guidelines.

Qualifications

• Proficient in SAS programming for clinical trials
• Experience with R programming for statistical analyses
• Knowledge of CDISC SDTM datasets and ADaM datasets
• Ability to oversee CRO programming deliverables
• Familiarity with regulatory submissions and DSURs

Responsibilities

• Generate SDTM/ADaM specs, datasets, reviewer’s guides and define.xml for multiple studies
• Develop SAS programs to create datasets, listings, tables, and graphs, collaborating with statisticians
• Deliver high-quality SAS and R programs tailored to clinical development programs
• Oversee CRO programming deliverables across studies to meet timelines
• Support preparation of CSRs, regulatory submissions, publications and exploratory analyses
• Adhere to FDA, GCP and electronic submission guidelines
• Contribute to standards for programming tools, outputs, and macros
• Develop CRFs, edit checks, and data validation plans
• Provide review of programming outputs

Skills

SAS

R programming

CDISC SDTM

ADaM

CRO oversight

Regulatory submissions

Tools

define.xml tooling

Job description

Cytel is seeking a Senior/Principal Statistical Programmer for a fully remote role. You will work on clinical development programs, implementing SDTM/ADaM specifications and generating complex datasets, tables, and figures in SAS and R.

You will also oversee CRO deliverables and contribute to regulatory submissions and exploratory analyses. The role requires senior-level expertise in statistical programming, with a focus on data standards, quality, and adherence to FDA guidelines.