Remote Principal Statistical Programmer (SAS + R)

Jobgether; Valladolid; Remote; EUR 70,000 - 90,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, dedicated to a sponsor within a global pharmaceutical client. You will independently drive programming activities across clinical development programs and oversee CRO programmers to ensure high-quality data outputs.

The role focuses on SAS and R program development, SDTM/ADaM specifications, and regulatory submission support, with adherence to FDA guidelines for electronic submissions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml files for multiple studies
• Develop SAS programs which generate datasets, complex listings, tables and graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs
• Oversee CROs' statistical programming deliverables to meet timelines
• Support the preparation of clinical study reports, regulatory submissions, publications, and exploratory analyses
• Understand and follow FDA regulations and guidelines for electronic submissions
• Contribute to standards for programming tools, outputs, and macros
• Assist in development of CRFs, edit check specifications, and data validation plans
• Provide review and/or author data transfer specifications for external vendor data
• Collaborate with internal and external functions to meet project timelines

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, dedicated to a sponsor within a global pharmaceutical client. You will independently drive programming activities across clinical development programs and oversee CRO programmers to ensure high-quality data outputs.

The role focuses on SAS and R program development, SDTM/ADaM specifications, and regulatory submission support, with adherence to FDA guidelines for electronic submissions.