Associate Director Biostatistics

Tipo Contratto: Da definire

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 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, SA Ps, CS Rs, 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 CR Os, 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 SO Ps



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 desirableA 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.

✔ Da definire