Attiva gli avvisi di lavoro via e-mail!

Statistician / Senior Statistician

Warman O'Brien

Monza

Ibrido

EUR 50.000 - 80.000

Tempo pieno

Ieri
Candidati tra i primi

Genera un CV personalizzato in pochi minuti

Ottieni un colloquio e una retribuzione più elevata. Scopri di più

Inizia da zero o importa un CV esistente

Descrizione del lavoro

Join a leading international pharmaceutical company as a Senior Biostatistician in Italy. This hybrid role involves leading statistical analysis and mentoring junior team members, applying advanced methodologies to support drug development while ensuring regulatory compliance. Candidates with a PhD or MS in a related field and strong proficiency in SAS, R, or Python are encouraged to apply.

Competenze

  • 3+ years’ experience with a PhD or 5+ years’ experience with an MS.
  • Proven experience in the pharmaceutical industry or CRO environment.
  • Familiarity with regulatory and HTA processes is a plus.

Mansioni

  • Lead the development and review of protocols and statistical analysis plans.
  • Mentor junior statisticians and contribute strategic insights.
  • Ensure regulatory readiness and high-quality outputs.

Conoscenze

Statistical methodologies
Communication skills
SAS
R
Python

Formazione

PhD in Biostatistics, Statistics, or related field
MS in Biostatistics, Statistics, or related field

Descrizione del lavoro

Senior Biostatistician – Global Pharma | Italy (Hybrid)

Shape the Future of Drug Development

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 Senior Biostatistician to join their dynamic and collaborative team. 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.

Applying advanced statistical methodologies and ensuring regulatory readiness of all deliverables.

Contributing strategic insights across clinical development, regulatory, market access, and medical affairs functions.

Mentoring junior statisticians and supporting team knowledge growth.

PhD (3+ years’ experience) or MS (5+ years’ experience) in Biostatistics, Statistics, or related field.

Proven experience in the pharmaceutical industry or CRO environment.

Strong proficiency in SAS , R , or Python .

Familiarity with regulatory and HTA (Health Technology Assessment) processes is highly desirable.

Strong communication skills, with the ability to translate complex data into actionable insights.

Flexible hybrid working model based in Italy.

Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.