Descrizione:
Experteer Overview: In this role you will design analysis plans and write specifications for analysis files, tables, listings and figures, and interpret analyses for study reports. You will develop and maintain programs to meet client needs, and mentor junior staff. You’ll coordinate with data management and other teams to ensure data quality and SOP compliance, while delivering high-quality deliverables on time. The position offers opportunities to lead small study work streams, contribute to SAPs and SN shell development, and engage with clients. This is a hands‑on Biostatistics role at IQVIA, combining programming, data scrutiny, and collaboration to improve study outcomes.Retribuzione / BenefitsPrepare analysis plans and write specifications for analysis files, tables, listings and figuresDevelop and maintain programs to meet client needs and SOP requirementsProduce high-quality deliverables with thorough validation and data checksProgram datasets and TLFs with consistency across outputsCreate and maintain study dashboards and indicatorsMentor junior staff and share knowledge within the teamSupport data management in CRF/database design and validation checksAuthor or review SAP and shells; write/maintain datasets and TLF specificationsQuality control of define.xml/SDTM/ADaM SDRG/ADRG as applicableMay serve as primary client contact and contribute to CSR and proposal discussionsResponsabilitàBachelor's Degree in Biostatistics or related field with 1+ year relevant experienceKnowledge of CDISC/ADaM/SDTM data standardsStrong planning, organizational, and multitasking abilitiesExcellent communication and interpersonal skillsAbility to manage conflicting priorities and work with clientsProficiency in SAS or R programming and ExcelUnderstanding of clinical drug development processExperience with data quality and SOP complianceRequisiti fondamentali• #J-18808-Ljbffr