Associate Director Biostatistics

Warman O'Brien; Bologna; Ibrido; EUR 80.000 - 110.000; Tempo pieno

Descrizione del lavoro

A globally renowned pharmaceutical company is seeking an experienced Associate Director / Director to lead the design of clinical trials and provide expert statistical input. This role involves ensuring compliance with regulatory frameworks and managing cross-functional project teams. Candidates should hold a PhD or MS with relevant industry experience and exceptional programming skills in SAS, R, or Python. The company offers a flexible hybrid work model based in Italy, creating a collaborative environment where you can make a significant impact on patient outcomes.

Servizi

Flexible working model

Impact on future medicine

Collaborative culture

Competenze

• 6+ years of industry experience with a PhD, or 8+ years with a MS.
• Proven ability to design and implement statistical analyses.
• Strong understanding of regulatory frameworks.

Mansioni

• Lead the design of clinical trials ensuring scientific robustness.
• Develop and review trial documentation including protocols and reports.
• Present findings to stakeholders clearly and effectively.
• Oversee multiple studies ensuring consistency and quality.

Conoscenze

Statistical analysis

SAS programming

Communication skills

Leadership

Collaboration

Formazione

PhD in Statistics, Biostatistics, or related field

MS in Statistics, Biostatistics, or related field

Strumenti

R

Python

Descrizione del lavoro

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

• 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 [e-mail] to learn more or apply today.