Associate Director Biostatistics

2 settimane fa

Bologna, Emilia-Romagna, Italia Warman O'Brien A tempo pieno

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.

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