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Associate Director Biostatistics

Remote / Online - Candidates ideally in
40139, Bologna, Emilia-Romagna, Italy
Listing for: Warman O'Brien
Remote/Work from Home position
Listed on 2026-01-01
Job specializations:
  • IT/Tech
    Data Security, Data Scientist, Data Analyst, Data Science Manager
Job Description & How to Apply Below
Associate Director / Director – Global Pharma Leader – Italy (Remote /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  Associate Director / Director  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, 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
Direct reports across large team

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 in Oncology or 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 / remote 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.
Position Requirements
10+ Years work experience
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