Remote Principal Statistical Programmer – SAS & R

Xometry Emea & Apac; Ibiza; A distancia; EUR 70.000 - 120.000; Jornada completa

Descripción de la vacante

Xometry Emea & Apac is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely embedded with a pharma client, supported by Cytel. The role focuses on delivering SDTM/ADaM specifications and leading CRO oversight across multiple trials.

You will develop and validate complex SAS and R programs, ensure regulatory compliance, and contribute to study reports and submissions. This is a sponsor-dedicated, high-autonomy position across global clinical programs.

Formación

• Senior statistical programmer with extensive experience in clinical development.
• Experience delivering SDTM/ADaM specs and programs.
• Experience overseeing CRO programmers and regulatory submissions.

Responsabilidades

• Generate SDTM and ADaM specifications, datasets, reviewer’s guides and define.xml files for multiple studies.
• Develop SAS programs to produce datasets, listings, tables and graphs for clinical trials.
• Deliver high-quality statistical programming results and maintain SAS and/or R programs.
• Oversee CRO programming deliverables and ensure timelines are met across studies.
• Support preparation of clinical study reports, regulatory submissions and publications.
• Ensure compliance with FDA regulations and good clinical practice for electronic submissions.
• Contribute to standards for programming tools, outputs, and macros.
• Participate in CRF development, edit check specs, and data validation plans.
• Provide review/author data transfer specifications for external vendor data.

Conocimientos

SAS

R

SDTM

ADaM

Clinical trials

GxP

Descripción del empleo

Xometry Emea & Apac is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely embedded with a pharma client, supported by Cytel. The role focuses on delivering SDTM/ADaM specifications and leading CRO oversight across multiple trials.

You will develop and validate complex SAS and R programs, ensure regulatory compliance, and contribute to study reports and submissions. This is a sponsor-dedicated, high-autonomy position across global clinical programs.