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Associate director biostatistics (montà)

Montà
Warman O'Brien
Pubblicato il 29 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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