Job Details
Manager Statistics
5641
Posted: 29/04/2025
Manager, Biostatistics – Global Pharma Leader – Italy (Hybrid)
What You’ll Be Doing
As a key member of the biostatistics team, you’ll:
What We’re Looking For
Why Join This Team?
- £Competitive
- , United Kingdom
- Permanent
Manager, Biostatistics – Global Pharma Leader – Italy (Hybrid)
Location: Italy – Hybrid
Sector: Pharmaceutical
Job Type: Permanent
Are you ready to take the next big step in your biostatistics career?
Our client, a globally renowned pharmaceutical company, is seeking a talented and experienced Manager of Biostatistics to join their high-impact team. If you thrive in a collaborative, fast-paced environment where your work directly contributes to groundbreaking treatments and improved patient outcomes, this could be your perfect fit.
What You’ll Be Doing
As a key member of the biostatistics team, you’ll:
- Lead the design of innovative clinical trials (Phases I–IV), ensuring they are efficient, scientifically robust, and aligned with strategic goals
- Develop and review key trial documentation: protocols, SAPs, CSRs, publications, and more
- Present statistical findings clearly and effectively to internal and external stakeholders
- Provide expert statistical input on regulatory submissions, publications, and responses to health authorities
- Oversee multiple studies within a therapeutic area, ensuring consistency, compliance, and quality
- Manage and maintain strong working relationships with CROs, vendors, and alliance partners
- Serve as the biostatistics point of contact across cross-functional project teams, contributing strategic insights throughout the drug development lifecycle
- Stay ahead of industry trends by applying statistical methodology to real-world evidence and market access initiatives
- Support audits and regulatory inspections, ensuring all deliverables are audit-ready and compliant with internal SOPs
What We’re Looking For
- PhD in Statistics, Biostatistics, or a related field with 6+ years of industry experience – OR – MS with 8+ years
- Strong hands-on programming experience in SAS, R, or Python
- Proven ability to design and implement advanced statistical analyses across all clinical phases
- Solid understanding of regulatory frameworks; experience with HTA is a plus
- Experience in rare disease trials is highly desirable
- A collaborative mindset with excellent communication and leadership skills
- Ability to lead, mentor, and guide junior statisticians and cross-functional teams
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 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?
Let’s talk! Reach out to Aimee at aimee@warmanobrien.com to learn more or apply today.

Aimee Weston
Principal Consultant in Biostatistics
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