17 set - Provincia di Reggio Emilia
Chiesi
Overview In this role you will lead SAS programming activities for clinical and safety data systems at Chiesi GRD, delivering high-quality data outputs for regulatory submissions. You will guide project-specific SAS work plans, maintain data integrity, and support SAP reviews and mock-up tables. You will collaborate across teams to ensure standardized data collection and compliant reporting, while driving best practices and data warehouse initiatives. This is a chance to shape data-driven decision making in a global rare diseases context and contribute to impactful therapies.
Retribuzione / Benefits
pension
private medical insurance
wellbeing programme
flexible benefits programme
relocation support
remote work options
Responsabilità
Establishes SAS programming needs for projects and develops work-plans to deliver outputs
Produces quality data outputs and preserves data integrity
Writes, validates, and maintains SAS programs for datasets, listings, tables, and graphs
Builds and maintains a library of SAS programs and related processes
Validates outputs and programs to support deliverables
Provides data collection and metadata package expertise for standardized submission-ready data
Contributes to SAP reviews and mock-up table/shell production
Develops standard edit checks and flags data issues indicating protocol adherence problems
Creates/adjusts processes to ensure CDISC-compliant submissions
Leads submission-related programming activities and oversees CRO programming activities
Maintains knowledge of regulatory requirements (GCP, GCDMP, CFR 21.11) and contributes to SOPs and work instructions
Supports data warehouse set-up and maintenance and develops novel tools to aid decision making
Requisiti fondamentali
~ Bachelor's Degree in a related field (Health Sciences, Statistics, Computer Science)
~7 years of Pharmaceutical/CRO experience
~ High level of SAS experience
~ Solid understanding of Data Management and Biostatistics processes
~ Experience cleaning/merging d
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