Business System Expert AXE

Excelya, Saclay, France

What our tracking knows about this posting

Published on 24 September 2026 · first appeared in our records on 24 September 2026.

Stable posting: first seen on 24 September 2026, with no abnormal reposting.

This posting shows no salary, while 12% of open postings in the same sector in this country (France) do.

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Join Excelya , where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role offers an exciting opportunity to support the analytical platforms used for the design and statistical analysis of clinical trial data. As a Business System Expert , you will act as the link between Biostatistics, Statistical Programming, IT, QA, and external vendors, ensuring the performance, compliance, and continuous improvement of critical clinical systems. Key Responsibilities • Provide functional support and administration for analytical platforms, primarily SAS (Viya, Grid, Clinical) and related systems. • Act as the main interface between Biostatisticians, SAS Programmers, IT teams, QA, and external providers. • Manage incidents, track technical issues, and coordinate resolution activities. • Ensure compliance and maintain Computer System Validation (CSV) documentation. • Develop and maintain quality documentation in accordance with GxP requirements. • Deliver training and support to end users. • Participate in system upgrades, deployments, and validation activities. • Monitor platform usage and propose corrective and preventive actions when needed. • Support the assessment and framing of new system implementation projects. • Master's degree in Life Sciences, Engineering, Computer Science, Statistics, or related field. • 2–5 years of experience in system administration, system support, or business systems management. • Proven experience with SAS platforms (SAS Viya, SAS Grid, SAS Analytics Platform, SAS Clinical). • Understanding of Biostatistics and Statistical Programming activities within clinical trials. • Experience with Computer System Validation (CSV) and validation documentation. • Knowledge of ICH-GCP, GxP, and clinical research processes . • Familiarity with Google Cloud is highly desirable. • Fluent English (written and spoken).

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