10 set - Sicilia
Warman O'Brien
Principal Biostatistician (strong Seniors considered) – Global Pharma | Italy (Hybrid) La preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa possibilità qui sotto.
Are you an experienced statistician ready to take your expertise to the next level? Our client, a leading international pharmaceutical company, is looking for a Principal Biostatistician 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.
You'll partner with cross-functional teams and external vendors to ensure the scientific integrity and success of clinical trials.
Designing innovative and efficient clinical trials (Phases I–IV), including defining study populations and endpoints aligned with key objectives.
Leading the development and review of protocols, statistical analysis plans (SAPs), study reports, and publication materials.
Presenting data and insights in a clear, concise,
and transparent manner to internal teams and regulatory bodies.
Serving as a statistical lead across multiple studies, ensuring high-quality, standardized outputs within a therapeutic area.
Contributing strategic insights across clinical development, regulatory, market access, and medical affairs functions.
Mentoring junior statisticians and supporting team knowledge growth.
Preparing for and supporting Health Authority inspections and audits.
PhD (6+ years' experience) or MS (8+ years' experience) in Biostatistics, Statistics, or related field.
Proven experience in the pharmaceutical industry or CRO environment.
Strong proficiency in SAS, R, or Python.
Deep understanding of statistical methodologies related to clinical trials and real-world evidence.
Experience in rare disease is a plus.
Familiarity with regulatory and HTA (Health Technology Assessment) processes is highly desirable.
Strong communication skills, with the
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