Principal Statistical Programmer (SAS + R) – Remote

Deel; Las Palmas de Gran Canaria; Remote; EUR 55,000 - 85,000; Full time

Job summary

Deel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, embedded with a pharmaceutical client. You will develop SDTM/ADaM, create datasets, listings, and graphs, and oversee CRO deliverables to ensure high-quality outputs for regulatory submissions.

You will implement reporting and analysis activities across multiple studies, ensuring compliance with GCP and FDA electronic submission standards, and contribute to study reports and exploratory analyses.

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 (including those with descriptive and standard inferential statistics in collaboration with a Statistician), and complex graphs
• Deliver high-quality statistical programming results including developing, validating, and maintaining SAS and/or R programs tailored to clinical development programs' needs
• Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet the pre-specified timelines
• Support the preparation of clinical study reports, regulatory submissions, publications, annual DSUR, and exploratory analyses
• Understand and follow FDA regulations which affect the reporting of clinical trial data. This includes good clinical practice and guidelines for electronic submissions.
• Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros
• Participate in the 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 (e.g. CROs, software vendors, clinical development partners, etc.) to ensure meeting project timelines and goals
• Provide review and

Job description

Deel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely, embedded with a pharmaceutical client. You will develop SDTM/ADaM, create datasets, listings, and graphs, and oversee CRO deliverables to ensure high-quality outputs for regulatory submissions.

You will implement reporting and analysis activities across multiple studies, ensuring compliance with GCP and FDA electronic submission standards, and contribute to study reports and exploratory analyses.