Senior Statistical Programmer

Warman O'Brien; Milano; Ibrido; EUR 90.000 - 150.000; Tempo pieno

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

Senior / Principal Biostatistician Statistical Programmer / Technology Lead - Global Pharma | Italy (Hybrid)

Shape the Future of Drug Development

Are you an experienced statistical programmer & technical lead, ready to take your expertise to the next level? Our client, a leading international pharmaceutical company, is looking for a Principal Biostatistician Statistical Programmer / Technology Lead to join their dynamic and collaborative team. The company are based in Italy, working hybrid (4 days to be based in office in Milan).

This position would require:

• Project & Team Leadership: Directs all programming activities for clinical trials (Phase I-IV) or large global projects, coordinating work across internal teams and external contractors.
• Regulatory Compliance: Ensures clinical data, analysis datasets, and reporting outputs strictly conform to global standards like CDISC standards (SDTM and ADaM)
• Technical Strategy & Innovation: Drives the integration of new technologies, automation tools, and programming languages (such as transitioning from traditional SAS to hybrid environments using R or Python and AI tools).
• Cross-Functional Collaboration: Partners closely with biostatisticians, data managers, and medical writers to design statistical analysis plans and resolve complex data issues.
• Resource & Quality Management: Allocates team workloads, sets project timelines, and mentors junior or senior programmers to ensure high technical standards.

Why Join This Team?

• Work with a top-tier pharmaceutical company with a global footprint
• Be part of a collaborative, science-driven culture
• Influence projects from early development through to regulatory approval
• Enjoy flexibility with a hybrid / remote work model based in Italy
• Make a tangible impact on the future of medicine – especially in rare and complex diseases

Ready to make a difference in your next role?