Principal Biostatistician (Oncology) - FSP

ppAs a bPrincipal Biostatistician /b, you will provide strategic statistical leadership for bOncology clinical trials /b, with a particular focus on bhematological malignancies /b including bmultiple myeloma, leukemia, and lymphoma /b. 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. /ph3Key Responsibilities /h3ulliProvide Principal-level Biostatistics leadership for Oncology clinical development programs and studies /liliLead and contribute to statistical activities across clinical trials, acting as the primary statistical representative on assigned studies /liliReview and provide quality control oversight of SDTM datasets and associated deliverables, ensuring compliance with CDISC standards /liliCollaborate closely with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure accurate and timely delivery of statistical outputs /liliSupport the interpretation and communication of study results to cross-functional stakeholders /liliEnsure all statistical deliverables meet quality, regulatory, and timeline expectations /liliEffectively communicate statistical concepts, analyses, and recommendations to both technical and non-technical audiences /liliContribute to study design discussions, protocol development, and statistical methodology as required /li /ulh3Candidate Requirements /h3ulliAdvanced experience as a bPrincipal Biostatistician /b within a Pharmaceutical, Biotechnology, or CRO environment /liliStrong experience within bOncology clinical development /b /liliDemonstrated expertise in bhematological malignancies /b, including bmultiple myeloma, leukemia, and/or lymphoma /b /liliStrong knowledge and practical application of bCDISC standards /b, including bSDTM /b /liliExperience performing or overseeing QC of SDTM datasets and related outputs /liliProven ability to work effectively within cross-functional teams and influence key stakeholders /liliExcellent verbal and written communication skills /liliStrong understanding of statistical principles and clinical trial methodology /li /ulh3Preferred Qualifications /h3ulliExperience serving as bLead Study Statistician /b within a cross-functional clinical development team /liliKnowledge and experience in bclinical trial statistical design /b and study planning /liliExperience supporting regulatory submissions and interactions with health authorities /liliFamiliarity with advanced statistical programming tools and industry-standard processes /li /ulpIQVIA 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 /ppIQVIA 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. 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. /p /p #J-18808-Ljbffr