Senior Statistician

Warman O'Brien; Latina; Ibrido; EUR 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

Warman O'Brien cherche à recruter un Senior Biostatistician pour rejoindre une entreprise pharmaceutique internationale. Dans ce rôle hybride, vous participerez activement à la conception d'essais cliniques, à la gestion des statistiques et à la présentation des résultats aux parties prenantes internes et externes, tout en offrant des opportunités de développement professionnel au sein d'une équipe dynamique.

Servizi

Flexibilité de travail

Rémunération compétitive

Opportunités de développement

Competenze

• PhD ou plus de 3 ans d'expérience en Biostatistique.
• Expérience démontrée dans l'industrie pharmaceutique ou en environnement CRO.
• Forte maîtrise de SAS, R ou Python.

Mansioni

• Concevoir des essais cliniques innovants et efficaces.
• Développer et revoir des protocoles et des plans d'analyse statistique.
• Mentorer des statisticiens juniors et soutenir la croissance des connaissances de l'équipe.

Conoscenze

SAS

R

Python

Statistical methodologies

Communication skills

Formazione

PhD in Biostatistics, Statistics, or related field

5 years' experience in pharmaceutical industry or CRO

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 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 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, based in Italy. Competitive compensation and development opportunities.

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