Programador Estadístico Principal SAS+R Remoto

Grup Bon Preu; Lérida; Remote; EUR 70,000 - 110,000; Full time

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to join our remote team supporting pharmaceutical clients. You will develop SAS programs, generate SDTM/ADaM outputs, and contribute to analysis reports and regulatory submissions.

Based in Spain or able to work remotely, you will collaborate with statisticians and CROs, ensure high-quality programming deliverables, and adhere to GCP and FDA/EMA guidelines. Experience leading programming efforts is a plus.

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
• Participate in overseeing CRO's statistical programming deliverables for multiple clinical studies to ensure high-quality and meet timelines
• Support the preparation of clinical study reports, regulatory submissions, publications, DSUR, and exploratory analyses
• Understand and follow FDA regulations which affect the reporting of clinical trial data
• 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

Job description

Cytel is seeking a Senior/Principal Statistical Programmer to join our remote team supporting pharmaceutical clients. You will develop SAS programs, generate SDTM/ADaM outputs, and contribute to analysis reports and regulatory submissions.

Based in Spain or able to work remotely, you will collaborate with statisticians and CROs, ensure high-quality programming deliverables, and adhere to GCP and FDA/EMA guidelines. Experience leading programming efforts is a plus.