OverviewIn 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 / Benefitspension
private medical insurance
wellbeing programme
flexible benefits programme
relocation support
remote work options
ResponsabilitàEstablishes 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 *****) and contributes to SOPs and work instructions
Supports data warehouse set-up and maintenance and develops novel tools to aid decision making
Requisiti fondamentaliBachelor'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 data from multiple sources
Experience creating and maintaining SAS reporting systems
Deep understanding of CDISC standards
Strong organizational and time-management skills
Ability to manage multiple priorities
Ability to work independently and in a team
SAS certification and/or A. Stat or P. Stat is an asset
English fluent
leadership
teamwork
problem-solving
SAS programming
Data management
CDISC standards

📌 Statistical Programmer (Parma)
🏢 Chiesi
📍 Parma