15 set - Roma
Iqvia
Descrizione dell’offerta di lavoro
Questa posizione è in IQVIA
Il processo di selezione sarà interamente gestito IQVIA.
Questa possibilità è disponibile in Reading - United Kingdom, Belgrade - Serbia, Rome - Italy, Paris - France, Vienna - Austria, Budapest - Hungary, Amsterdam - Netherlands, Dublin - Ireland, Sofia - Bulgaria, Frankfurt - Germany, Athens - Greece, Ljubljana - Slovenia, Madrid - Spain, Brussels - Belgium, Bratislava - Slovakia, Prague - Czech Republic, Copenhagen - Denmark, Stockholm - Sweden.
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As a Principal Biostatistician , you will provide strategic statistical leadership for Oncology clinical trials , with a particular focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma . You will work closely with cross-functional teams to deliver high-quality statistical support across the clinical development lifecycle, ensuring compliance with regulatory and industry standards.
Key Responsibilities
Provide Principal-level Biostatistics leadership for Oncology clinical development programs and studies
Lead and contribute to statistical activities across clinical trials, acting as the primary statistical representative on assigned studies
Review and provide quality control oversight of SDTM datasets and associated deliverables , ensuring compliance with CDISC standards
Collaborate closely with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure accurate and timely delivery of statistical outputs
Support the interpretation and communication of study results to cross-functional stakeholders
Ensure all statistical deliverables meet quality, regulatory, and timeline expectations
Effectively communicate statistical concepts, analyses, and recommendations to both technical and non-technical audiences
Contribute to study design discussions, protocol development, and statistical methodology as required
Candidate Requirements
Advanced experience as a Principal Biostatistician within a Pharm
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