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Associate director biostatistics

San Rocco al Porto
Contratto a tempo indeterminato
Warman O'Brien
Pubblicato il Pubblicato 23h fa
Descrizione

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 DoingAs 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 teamWhat 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 teamsWhy 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 aimee@warmanobrien.com to learn more or apply today.

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