Statistical Programmer
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 / Benefits
pensionprivate medical insurancewellbeing programmeflexible benefits programmerelocation supportremote work options
Responsabilità
Establishes SAS programming needs for projects and develops work-plans to deliver outputsProduces quality data outputs and preserves data integrityWrites, validates, and maintains SAS programs for datasets, listings, tables,
and graphsBuilds and maintains a library of SAS programs and related processesValidates outputs and programs to support deliverablesProvides data collection and metadata package expertise for standardized submission-ready dataContributes to SAP reviews and mock-up table/shell productionDevelops standard edit checks and flags data issues indicating protocol adherence problemsCreates/adjusts processes to ensure CDISC-compliant submissionsLeads submission-related programming activities and oversees CRO programming activitiesMaintains knowledge of regulatory requirements (GCP, GCDMP, CFR 21.11) and contributes to SOPs and work instructionsSupports 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 experienceHigh level of SAS experienceSolid understanding of Data Management and Biostatistics processesExperience cleaning/merging data from multiple sourcesExperience creating and maintaining SAS reporting systemsDeep understanding of CDISC standardsStrong organizational and time-management skillsAbility to manage multiple prioritiesAbility to work independently and in a teamSAS certification and/or A. Stat or P. Stat is an assetEnglish fluentleadershipteamworkproblem-solvingSAS programmingData managementCDISC standards
Retribuzione / Benefits
pensionprivate medical insurancewellbeing programmeflexible benefits programmerelocation supportremote work options
Responsabilità
Establishes SAS programming needs for projects and develops work-plans to deliver outputsProduces quality data outputs and preserves data integrityWrites, validates, and maintains SAS programs for datasets, listings, tables,
and graphsBuilds and maintains a library of SAS programs and related processesValidates outputs and programs to support deliverablesProvides data collection and metadata package expertise for standardized submission-ready dataContributes to SAP reviews and mock-up table/shell productionDevelops standard edit checks and flags data issues indicating protocol adherence problemsCreates/adjusts processes to ensure CDISC-compliant submissionsLeads submission-related programming activities and oversees CRO programming activitiesMaintains knowledge of regulatory requirements (GCP, GCDMP, CFR 21.11) and contributes to SOPs and work instructionsSupports 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 experienceHigh level of SAS experienceSolid understanding of Data Management and Biostatistics processesExperience cleaning/merging data from multiple sourcesExperience creating and maintaining SAS reporting systemsDeep understanding of CDISC standardsStrong organizational and time-management skillsAbility to manage multiple prioritiesAbility to work independently and in a teamSAS certification and/or A. Stat or P. Stat is an assetEnglish fluentleadershipteamworkproblem-solvingSAS programmingData managementCDISC standards