Senior Biostatistician & Tech Lead — Hybrid (Italy)

Warman O'Brien

Milano

Ibrido

EUR 90.000 - 150.000

Tempo pieno

39 ore fa
Candidati tra i primi
Generatore di candidature

Distinguiti per questo ruolo — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Hybrid/Remote work model in Italy

Descrizione del lavoro

Warman O'Brien seeks an experienced Principal Biostatistician Statistical Programmer / Technology Lead to shape drug development and lead programming for global trials in a hybrid Italy-based setting (Milan). The role emphasizes CDISC SDTM/ADaM compliance, regulatory readiness, and driving technical innovation with SAS, R, Python, and AI tools.

You will partner with biostatisticians, data managers, and medical writers to design analysis plans and oversee data integrity, quality, and project

Competenze

  • Directs all programming activities for clinical trials (Phase I-IV) or large global projects.
  • Ensures clinical data, analysis datasets, and reporting outputs conform to global standards like CDISC (SDTM and ADaM).
  • Drives integration of new technologies and automation tools, incl. transitioning from SAS to hybrid environments using R/Python and AI tools.

Mansioni

  • Directs all programming activities for clinical trials across Phase I–IV or large global projects.
  • Ensures SDTM/ADaM data standards compliance for datasets and outputs.
  • Leads the adoption of new technologies and automation tools (R/Python, AI) in programming.
  • Partners with biostatisticians, data managers and medical writers to shape analysis plans.
  • Mentors junior or senior programmers to uphold technical standards.

Conoscenze

Project Leadership
Regulatory Compliance
Technical Strategy
Cross-Functional Collaboration
Mentoring

Strumenti

SAS
R
Python
AI tools

Descrizione del lavoro

Warman O'Brien seeks an experienced Principal Biostatistician Statistical Programmer / Technology Lead to shape drug development and lead programming for global trials in a hybrid Italy-based setting (Milan). The role emphasizes CDISC SDTM/ADaM compliance, regulatory readiness, and driving technical innovation with SAS, R, Python, and AI tools.

You will partner with biostatisticians, data managers, and medical writers to design analysis plans and oversee data integrity, quality, and project

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