Requirements: English
Company: Warman O''Brien
Region: Turin , Piedmont
Manager, Biostatistics (Associate Director) Global Pharma Leader Italy (Hybrid)
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 ground-breaking treatments and improved patient outcomes, this could be your perfect fit.
What Youll Be Doing
As a key member of the biostatistics team, youll:
- Lead the design of innovative clinical trials (Phases IIV), 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 Were 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?
Lets talk! Reach out to Aimee at to learn more or apply today.