Rwe Biostatistician H / F

Astek; Boulogne-Billancourt; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading CRO in the pharmaceutical sector is seeking a Senior Preclinical Biostatistician to work on real-world evidence projects. Responsibilities include designing statistical analyses, contributing to analysis plans, and collaborating with cross-functional teams. A Master's or PhD in Biostatistics is required, along with experience in RWE and proficiency in SAS.

Qualifications

• Holder of a Master's / PhD in Biostatistics, Applied Statistics, or related field.
• Experienced in RWE / epidemiology / pharmacoepidemiology.
• Skilled in SAS and familiar with clinical reporting and regulatory standards.

Responsabilités

• Design, develop, and perform statistical analyses on observational and RWE datasets.
• Contribute to the development of statistical analysis plans.
• Collaborate with cross-functional teams.

Connaissances

Statistical analysis

SAS

Epidemiology

Formation

Master's / PhD in Biostatistics or Applied Statistics

Outils

R

Description du poste

Alsinova, the Astek Group subsidiary offering a complete CRO solution, is recruiting a Senior Preclinical Biostatistician for a project in the pharmaceutical sector.

Your mission (should you decide to accept it) :

As part of a strategic collaboration with a leading healthcare company, we are looking for an experienced RWE Biostatistician to contribute to real-world evidence projects.

Your daily activities will be :

Design, develop, and perform statistical analyses on observational and RWE datasets.

Contribute to the development of statistical analysis plans and draft corresponding protocol and report sections.

Support the implementation and monitoring of data surveillance plans.

Ensure quality, robustness, and interpretation of statistical outputs.

Perform exploratory analyses and address additional requests from health authorities or internal stakeholders.

Collaborate closely with cross‑functional teams including epidemiology, data science, clinical, and regulatory affairs.

You :

• Holder of a Master's / PhD in Biostatistics, Applied Statistics, or related field
• Experienced in RWE / epidemiology / pharmacoepidemiology, ideally in a pharma, biotech, or CRO environment.
• Skilled in SAS (knowledge of R is a plus) and familiar with clinical reporting and regulatory standards.