Senior Biostatistician: Lead Analyses for Clinical Programs

Recordati; Lombardia; On-site; EUR 59,000 - 72,000; Full time

Job summary

Recordati is seeking an experienced Senior Biostatistician to provide expert methodological support across development portfolios, ensuring robust analysis and regulatory-ready statistical input. You will contribute to statistical strategy, promote modern methods, and uphold high standards across R&D.

You will lead analyses, interact with cross-functional teams, and maintain hands-on SAS skills while guiding external partners. Fluency in English and collaboration across regions are essential.

Qualifications

• Typically 10+ years of progressive biostatistics experience in pharma/biotech/CRO.

Responsibilities

• Define robust statistical approaches for clinical trials and evidence plans.
• Provide statistical direction to cross-functional project teams throughout development.
• Prepare high-quality input to development plans, protocols, data management plans and study reports.
• Lead complex analyses and communicate implications to stakeholders.
• Maintain hands-on SAS expertise and oversee programming from partners.
• Collaborate with Medical Writing and other functions for regulatory readiness.
• Oversee CROs and study sites to ensure data integrity and quality.

Skills

Biostatistics

GCP

CDISC

SAS

Regulatory submissions

Education

Advanced degree in Statistics

PhD advantageous

Tools

SAS

Job description

Recordati is seeking an experienced Senior Biostatistician to provide expert methodological support across development portfolios, ensuring robust analysis and regulatory-ready statistical input. You will contribute to statistical strategy, promote modern methods, and uphold high standards across R&D.

You will lead analyses, interact with cross-functional teams, and maintain hands-on SAS skills while guiding external partners. Fluency in English and collaboration across regions are essential.