Statistics Manager

Warman O'Brien; Madrid; Presencial; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a skilled Manager of Biostatistics to join their innovative team. This role offers the opportunity to lead the design of clinical trials, ensuring they are scientifically robust and aligned with strategic goals. You will work closely with cross-functional teams, providing expert statistical input on regulatory submissions and influencing projects from early development through to approval. With a flexible hybrid work model, you will make a significant impact on the future of medicine, especially in rare and complex diseases. Join a collaborative, science-driven culture and thrive in a fast-paced environment.

Formación

• 6+ years of industry experience with a PhD or 8+ years with an MS.
• Strong programming skills in SAS, R, or Python.

Responsabilidades

• Lead the design of clinical trials and ensure compliance with strategic goals.
• Present statistical findings to stakeholders and manage relationships with CROs.

Conocimientos

SAS

R

Python

Statistical Analysis

Regulatory Frameworks

Leadership

Communication Skills

Educación

PhD in Statistics or Biostatistics

MS in Statistics or Biostatistics

Descripción del empleo

Sector : Pharmaceutical

Job Type : Permanent

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.

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

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?