Senior Statistician

Warman O'Brien; Verona; Ibrido; EUR 45.000 - 70.000; Tempo pieno

Descrizione del lavoro

A leading international pharmaceutical company is seeking a Senior Biostatistician to design and implement innovative clinical trials in a hybrid work environment based in Italy. This role requires a strong background in statistics and the ability to collaborate with cross-functional teams to influence global health outcomes. Candidates should be proficient in statistical tools and have significant experience in the pharmaceutical industry. Join a dynamic team committed to improving health outcomes and advance your career.

Servizi

Flexible working arrangements

Competitive compensation

Development opportunities

Competenze

• Proven experience in the pharmaceutical industry or CRO environment.
• Strong proficiency in SAS, R, or Python.
• Experience in rare diseases is a plus.

Mansioni

• Design and lead clinical trials across all phases, ensuring scientific integrity.
• Develop protocols and statistical analysis plans, and present insights to teams.
• Mentor junior statisticians and manage Biostatistics deliverables.

Conoscenze

SAS

R

Python

Statistical methodologies

Communication skills

Formazione

PhD in Biostatistics or related field

3+ years of experience in Biostatistics

5+ years of experience in pharmaceuticals

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:

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

What We’re Looking For

PhD or 3+ years’ experience in Biostatistics, Statistics, or related field, or 5+ years’ experience. 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 diseases 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, based in Italy. Competitive compensation and development opportunities.

Interested? Reach out to Aimee directly at [contact information] to learn more or apply confidentially.