14 ott - Milano
Warman O'Brien
ph3bPrincipal Biostatistician (strong Seniors considered) – Global Pharma | Italy (Hybrid) /b /h3 h3bShape the Future of Drug Development /b /h3 pAre 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.
/p h3bWhat You'll Be Doing /b /h3 pAs 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.
/p h3bYour responsibilities will include: /b /h3 ul liDesigning innovative and efficient clinical trials (Phases I–IV), including defining study populations and endpoints aligned with key objectives.
/li liLeading the development and review of protocols, statistical analysis plans (SAPs), study reports, and publication materials.
/li liPresenting data and insights in a clear, concise, and transparent manner to internal teams and regulatory bodies.
/li liServing as a statistical lead across multiple studies, ensuring high-quality, standardized outputs within a therapeutic area.
/li liActing as a primary point of contact for CROs and vendors, managing Biostatistics deliverables end-to-end.
/li liApplying advanced statistical methodologies and ensuring regulatory readiness of all deliverables.
/li liContributing strategic insights across clinical development, regulatory, market access, and medical affairs functions.
/li liMentoring junior statisticians and supporting team knowledge growth.
/liliPreparing for and supporting Health Authority inspections and audits.
/li /ul h3bWhat We're Looking For /b /h3 ul libPhD /b (6+ years' experience) or bMS /b (8+ years' experience) in Biostatistics, Statistics, or related field.
/li liProven experience in the pharmaceutical industry or CRO environment.
/liliStrong proficiency in bSAS /b, bR /b, or bPython /b.
/li liDeep understanding of statistical methodologies related to clinical trials and real-world evidence.
/li liExperience in rare disease is a plus.
/li liFamiliarity 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 /ul h3bWhy Join This Team?
/b /h3 ul liWork with a top-tier pharmaceutical company with a global footprint /li liBe part of a collaborative, science-driven culture /li liInfluence projects from early development through to regulatory approval /li liEnjoy flexibility with a bhybrid / remote work model /b based in Italy /li liMake a tangible impact on the future of medicine – especially in brare and complex diseases /b /li /ul pReady to make a difference in your next role?
/p /p #J-*****-Ljbffr
17 ott - Varese
Callimacus
17 ott - Modena
Seedtag
17 ott - Mantova
Novocure
17 ott - Chieti
Teoresi Group