09 set - Roma
Warman O'Brien
pstrongPrincipal Biostatistician (strong Seniors considered) – Global Pharma | Italy (Hybrid) /strong /ppbr / /ppstrongShape the Future of Drug Development /strong /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 strongPrincipal Biostatistician /strong 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 / /ppstrongWhat You’ll Be Doing /strong /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 / /ppstrongYour responsibilities will include: /strong /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 / /ppstrongWhat We’re Looking For /strong /pullistrongPhD /strong (6+ years’ experience) or strongMS /strong (8+ years’ experience) in Biostatistics, Statistics, or related field. /liliProven experience in the pharmaceutical industry or CRO environment. /liliStrong proficiency in strongSAS /strong, strongR /strong, or strongPython /strong. /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 / /ppstrongWhy Join This Team? /strong /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 stronghybrid / remote work model /strong based in Italy /liliMake a tangible impact on the future of medicine – especially in strongrare and complex diseases /strong /li /ulpbr / /pp strongReady to make a difference in your next role? /strong /ppLet’s talk! Reach out to strongAimee at /strong to learn more or apply today. /ppbr / /p
10 set - Milano
During S.p.A. Filiale di Milano Cadorna
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agap2 Italia