Principal Statistician

pbPrincipal Biostatistician (strong Seniors considered) – Global Pharma | Italy (Hybrid) /b /ppbr/ppbShape the Future of Drug Development /b /ppbr/ppAre you an experienced statistician ready to take your expertise to the next level? Our client, a leading international pharmaceutical company, is looking for a bPrincipal Biostatistician /b to join their dynamic and collaborative team. If you're passionate about designing meaningful clinical trials and influencing global health outcomes, this is the opportunity for you. /ppbr/ppbWhat You’ll Be Doing /b /ppAs a key statistical expert, you’ll play a pivotal role across all phases of clinical development—from strategy through execution. You’ll partner with cross-functional teams and external vendors to ensure the scientific integrity and success of clinical trials. /ppbr/ppbYour responsibilities will include: /b /pulliDesigning innovative and efficient clinical trials (Phases I–IV), including defining study populations and endpoints aligned with key objectives. /liliLeading the development and review of protocols, statistical analysis plans (SAPs), study reports, and publication materials. /liliPresenting data and insights in a clear, concise, and transparent manner to internal teams and regulatory bodies. /liliServing as a statistical lead across multiple studies, ensuring high-quality, standardized outputs within a therapeutic area. /liliActing as a primary point of contact for CROs and vendors, managing Biostatistics deliverables end-to-end. /liliApplying advanced statistical methodologies and ensuring regulatory readiness of all deliverables. /liliContributing strategic insights across clinical development, regulatory, market access, and medical affairs functions. /liliMentoring junior statisticians and supporting team knowledge growth. /liliPreparing for and supporting Health Authority inspections and audits. /li /ulpbr/ppbWhat We’re Looking For /b /pullibPhD /b (6+ years’ experience) or bMS /b (8+ years’ experience) in Biostatistics, Statistics, or related field. /liliProven experience in the pharmaceutical industry or CRO environment. /liliStrong proficiency in bSAS /b, bR /b, or bPython /b. /liliDeep understanding of statistical methodologies related to clinical trials and real-world evidence. /liliExperience in rare disease is a plus. /liliFamiliarity with regulatory and HTA (Health Technology Assessment) processes is highly desirable. /liliStrong communication skills, with the ability to translate complex data into actionable insights. /li /ulpbr/ppbWhy Join This Team? /b /pulliWork with a top-tier pharmaceutical company with a global footprint /liliBe part of a collaborative, science-driven culture /liliInfluence projects from early development through to regulatory approval /liliEnjoy flexibility with a bhybrid / remote work model /b based in Italy /liliMake a tangible impact on the future of medicine – especially in brare and complex diseases /b /li /ulpbr/pp bReady to make a difference in your next role? /b /ppLet’s talk! Reach out to bAimee at /b to learn more or apply today. /ppbr/p