Senior Statistician

PotisEdge; Torino; Ibrido; EUR 50.000 - 80.000; Tempo pieno

Descrizione del lavoro

A leading international pharmaceutical company is seeking a Senior Biostatistician to join their team in Italy. In this hybrid role, you will be instrumental in designing and leading clinical trials across all phases. The ideal candidate will have a PhD or MS in Biostatistics, with significant experience in the pharmaceutical sector. You will also need strong analytical and communication skills to present insights effectively. This position offers competitive compensation and the chance to collaborate with global experts to influence health outcomes.

Servizi

Flexible hybrid working model

Competitive compensation

Development opportunities

Competenze

• 3+ years of experience in Biostatistics for PhD or 5+ years for MS.
• Experience in the pharmaceutical industry or CRO environment.
• Familiarity with regulatory and HTA processes.

Mansioni

• Design innovative and efficient clinical trials (Phases I–IV).
• Lead the development and review of statistical analysis plans.
• Present data clearly to internal teams and regulatory bodies.

Conoscenze

Advanced statistical methodologies

Proficiency in SAS

Proficiency in R

Proficiency in Python

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

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