Senior Principal Statistical Programmer - SAS & R (Remote)

Ethos; Santiago de Compostela; Remote; EUR 70,000 - 110,000; Full time

Benefits offered by this job

Remote work option

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to join a sponsor-dedicated team embedded with a global pharmaceutical client. You will independently lead programming activities for multiple studies, delivering high-quality SDTM/ADaM datasets, tables, listings and figures with minimal supervision.

You will oversee CRO programming deliverables, ensure regulatory compliance with FDA guidelines, and contribute to standards and specifications for data transfer and reporting.

Qualifications

• Senior/Principal Statistical Programmer with experience in clinical trials.
• Experience collaborating with CROs and external vendors.
• Knowledge of FDA regulations and electronic submissions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml for multiple studies.
• Develop SAS programs for datasets, listings, tables and graphs.
• Deliver high-quality statistical programming results using SAS and/or R.
• Oversee CRO programming deliverables and ensure timelines.
• Support preparation of clinical study reports, regulatory submissions and exploratory analyses.
• Contribute to standards for programming tools, outputs, and macros.
• Develop CRFs, edit checks, and data validation plans.
• Coordinate data transfer specifications with external vendors.
• Collaborate with internal/external functions to meet project goals.

Skills

SAS programming

R programming

SDTM/ADaM

Clinical data reporting

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to join a sponsor-dedicated team embedded with a global pharmaceutical client. You will independently lead programming activities for multiple studies, delivering high-quality SDTM/ADaM datasets, tables, listings and figures with minimal supervision.

You will oversee CRO programming deliverables, ensure regulatory compliance with FDA guidelines, and contribute to standards and specifications for data transfer and reporting.