SAS Data Programmer

4 giorni fa
Provincia di Reggio nell'Emilia, Emilia-Romagna, Italia Chiesi Tempo pieno
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 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

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