Senior Statistician

**Senior Biostatistician – Global Pharma | North 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
**Biostatistician**
/
**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.
- 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 (FSP Ideal).
- Strong proficiency in
**SAS**
,
**R**
, or
**Python**
.
- Deep understanding of statistical methodologies related to clinical trials and real-world evidence.
- Experience in rare disease / oncology is a plus.
- Experience with Data Visualisation / Exploration is highly desired.
- 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
**aimee@warmanobrien.com**
to learn more or apply confidentially.