Senior/Principal Statistical Programmer (Remote) - SAS + R

Stantec Consulting International Ltd.; Salamanca; Remote; EUR 70,000 - 95,000; Full time

Job summary

Stantec Consulting International Ltd. seeks a Senior/Principal Statistical Programmer SAS + R for remote work with a major pharmaceutical sponsor.

You will lead statistical programming activities across multiple studies, oversee CRO deliverables, and contribute to regulatory submissions while ensuring data quality and compliance with GCP. The role involves developing SDTM/ADaM outputs, complex listings, tables, and graphs, and collaborating with statisticians to deliver high-quality results in a

Qualifications

• Extensive experience in clinical development programming.
• Ability to lead CROs and coordinate cross-functional teams.
• Knowledge of FDA regulations and GCP for regulatory submissions.

Responsibilities

• Generate SDTM/ADaM specifications, datasets, reviewer’s guides and define.xml files.
• Develop SAS programs for datasets, listings, tables and graphs.
• Deliver high-quality SAS and R programs tailored to clinical development needs.
• Oversee CRO deliverables and ensure timelines are met.
• Support preparation of clinical study reports and regulatory submissions.
• Contribute to development and maintenance of programming standards.

Skills

SAS programming

R programming

SDTM/ADaM

Regulatory submissions support

CRO oversight

Tools

define.xml development

CDISC standards

Job description

Stantec Consulting International Ltd. seeks a Senior/Principal Statistical Programmer SAS + R for remote work with a major pharmaceutical sponsor.

You will lead statistical programming activities across multiple studies, oversee CRO deliverables, and contribute to regulatory submissions while ensuring data quality and compliance with GCP. The role involves developing SDTM/ADaM outputs, complex listings, tables, and graphs, and collaborating with statisticians to deliver high-quality results in a