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 / Benefits Prepare analysis plans and write specifications for analysis files, tables, listings and figures
Develop and maintain programs to meet client needs and SOP requirements
Produce high-quality deliverables with thorough validation and data checks
Program datasets and TLFs with consistency across outputs
Create and maintain study dashboards and indicators




Mentor junior staff and share knowledge within the team
Support data management in CRF/database design and validation checks
Author or review SAP and shells; write/maintain datasets and TLF specifications
Quality control of define.xml/SDTM/ADaM SDRG/ADRG as applicable
May serve as primary client contact and contribute to CSR and proposal discussions
Responsabilità Bachelor's Degree in Biostatistics or related field with 1+ year relevant experience
Knowledge of CDISC/ADaM/SDTM data standards
Strong planning, organizational, and multitasking abilities
Excellent communication and interpersonal skills
Ability to manage conflicting priorities and work with clients
Proficiency in SAS or R programming and Excel
Understanding of clinical drug development process
Experience with data quality and SOP compliance
Requisiti fondamentali •
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📌 Biostatistician (Italia)
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📍 Italia