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.La preghiamo di leggere attentamente la seguente descrizione del lavoro per assicurarsi di essere la persona giusta per questo ruolo prima di candidarsi.Key ResponsibilitiesProvide Principal-level Biostatistics leadership for Oncology clinical development programs and studiesLead and contribute to statistical activities across clinical trials, acting as the primary statistical representative on assigned studiesReview and provide quality control oversight of SDTM datasets and associated deliverables, ensuring compliance with CDISC standardsCollaborate closely with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure accurate and timely delivery of statistical outputsSupport the interpretation and communication of study results to cross-functional stakeholdersEnsure all statistical deliverables meet quality, regulatory, and timeline expectationsEffectively communicate statistical concepts, analyses, and recommendations to both technical and non-technical audiencesContribute to study design discussions, protocol development, and statistical methodology as requiredCandidate RequirementsAdvanced experience as a Principal Biostatistician within a Pharmaceutical, Biotechnology,



or CRO environmentStrong experience within Oncology clinical developmentDemonstrated expertise in hematological malignancies, including multiple myeloma, leukemia, and/or lymphomaStrong knowledge and practical application of CDISC standards, including SDTMExperience performing or overseeing QC of SDTM datasets and related outputsProven ability to work effectively within cross-functional teams and influence key stakeholdersExcellent verbal and written communication skillsStrong understanding of statistical principles and clinical trial methodologyPreferred QualificationsExperience serving as Lead Study Statistician within a cross-functional clinical development teamKnowledge and experience in clinical trial statistical design and study planningExperience supporting regulatory submissions and interactions with health authoritiesFamiliarity with advanced statistical programming tools and industry-standard processesIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. xysqume Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.#J-18808-Ljbffr

📌 Principal Biostatistician (Oncology) - Fsp (Roma)
🏢 Iqvia
📍 Roma