Senior Statistician

Warman O'Brien; Ancona; Ibrido; EUR 65.000 - 90.000; Tempo pieno

Descrizione del lavoro

A top-tier global pharmaceutical company seeks a Senior Biostatistician to play a critical role in clinical trial design and execution. This position allows you to shape drug development while collaborating with industry experts and ensuring regulatory compliance. With a flexible hybrid model and competitive compensation, this role provides a great opportunity for professional growth.

Servizi

Collaborative work with global experts

Flexible working model

Competitive compensation

Development opportunities

Competenze

• 3+ years of experience with a PhD or 5+ years with an MS in Biostatistics.
• Proven pharmaceutical industry experience.
• Experience in rare diseases is a plus.

Mansioni

• Design innovative clinical trials and lead protocol development.
• Serve as a statistical lead across multiple studies.
• Mentor junior statisticians and ensure data integrity.

Conoscenze

Proficiency in SAS

Proficiency in R

Proficiency in Python

Statistical methodologies

Strong communication skills

Formazione

PhD in Biostatistics or related field

MS in Biostatistics or related field

Descrizione del lavoro

Senior Biostatistician – Global Pharma | Italy (Hybrid)

Shape the Future of Drug Development

Are you an experienced statistician ready to take your expertise to the next level? Our client, a leading international pharmaceutical company, is looking for a Senior Biostatistician to join their dynamic and collaborative team. If you're passionate about designing meaningful clinical trials and influencing global health outcomes, this is the opportunity for you.

What You’ll Be Doing

As a key statistical expert, you’ll play a pivotal role across all phases of clinical development—from strategy through execution. You’ll partner with cross-functional teams and external vendors to ensure the scientific integrity and success of clinical trials.

Your responsibilities will include :

• Designing innovative and efficient clinical trials (Phases I–IV), including defining study populations and endpoints aligned with key objectives.
• Leading the development and review of protocols, statistical analysis plans (SAPs), study reports, and publication materials.
• Presenting data and insights in a clear, concise, and transparent manner to internal teams and regulatory bodies.
• Serving as a statistical lead across multiple studies, ensuring high-quality, standardized outputs within a therapeutic area.
• Acting as a primary point of contact for CROs and vendors, managing Biostatistics deliverables end-to-end.
• Applying advanced statistical methodologies and ensuring regulatory readiness of all deliverables.
• Contributing strategic insights across clinical development, regulatory, market access, and medical affairs functions.
• Mentoring junior statisticians and supporting team knowledge growth.
• Preparing for and supporting Health Authority inspections and audits.

What We’re Looking For

• PhD (3+ years’ experience) or MS (5+ years’ experience) in Biostatistics, Statistics, or related field.
• Proven experience in the pharmaceutical industry or CRO environment.
• Strong proficiency in SAS , R , or Python .
• Deep understanding of statistical methodologies related to clinical trials and real-world evidence.
• Experience in rare disease is a plus.
• Familiarity with regulatory and HTA (Health Technology Assessment) processes is highly desirable.
• Strong communication skills, with the ability to translate complex data into actionable insights.

Why Join?

• Collaborate with global experts on innovative clinical programs.
• Play a strategic role in improving health outcomes across diverse therapeutic areas.
• Flexible hybrid working model based in Italy.
• Competitive compensation and development opportunities.

Interested?

Reach out to Aimee directly at to learn more or apply confidentially.