CareerPlan

Biostatistician

Leuven, BelgiumFull-time2026-07-06 → 2026-11-10
On-site

Core

Design and execute statistical analyses for clinical trials to support the development of safe and effective medical therapeutics.

Role type

Biostatistician

Builds

Clinical trial statistical reports and analysis plans

Domain

Pharmaceutical clinical research

Required skills

SAS programming, statistical methodology design, clinical trial protocol review, database design, statistical reporting

Preferred skills

Pharmaceutical or CRO industry experience

Technologies

SAS

Responsibilities

Contribute to clinical development plan preparation; Review study protocols and prepare statistical methodologies; Program study analysis and prepare statistical methods sections for reports; Communicate requirements for CRF and database design; Communicate statistical results to medical writing personnel

Seniority

Mid-level, hands-on IC