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Associate director biostatistics

Contratto a tempo indeterminato
Warman O'Brien
Pubblicato il 22 settembre
Descrizione

Overview

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.

Direct message the job poster from Warman O'Brien

What You’ll Be Doing

* 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 to learn more or apply today.

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