Biostatistician

Allis Na; Bordeaux; Hybride; EUR 45 000 - 65 000; Plein temps

Résumé du poste

A consulting company in healthcare is seeking a Biostatistician (M/F) for a full-time permanent position in Bordeaux. You will manage statistical projects across various therapeutic areas, requiring strong biostatistics and programming skills. A Master or PhD in applied statistics is essential, along with 2-3 years of relevant experience in a CRO, pharma, or academic environment. Proficiency in French and English is required, in addition to skills in SAS and R.

Qualifications

• At least 2-3 years of relevant experience as a biostatistician in a CRO, pharma, or academic environment.
• Experience in real-world studies or clinical studies.
• Good knowledge of regulatory standards (ICH, FDA, EMA, ENCEPP, HAS).

Responsabilités

• Writing and critical reviewing of study documentation on statistics.
• Implementation of relevant and well-adapted statistical analyses.
• Ensuring quality standards and timelines for deliverables.
• Participate in discussions shaping future projects and results valorization.
• Draft or contribute to standard operating procedures related to statistics.
• Continuously update statistical skills to stay current with scientific progress.

Connaissances

Biostatistics

Statistical programming

Office suites

Team spirit

Autonomy

Team spirit

Formation

Master or PhD in applied statistics

Outils

SAS

R

Office suite

Description du poste

Horiana is a consulting company dedicated to epidemiology and biostatistics, designing and conducting real world healthcare studies. Horiana aims to support its clients - private and public/academic professionals in the healthcare field - at all stages of their projects.

Horiana is currently expanding its team with a full-time permanent position for a biostatistician (M/F). The position is based in Bordeaux (33) or remotely, depending on the profile of the candidate.

Within the Primary Databases department, you will be in charge of statistical projects in various therapeutical areas based on primary research or secondary databases. You will also be involved in other steps of the study (preparing responses to requests for proposals, design & analyses conception, meetings, dissemination of results). Strong skills in biostatistics and programming are required.

Profile

• A master or PhD degree in applied statistics in the fields of health and life sciences
• At least 2-3 years of relevant experience as a biostatistician in a CRO, pharma or academic environment
• Experience in RWS or clinical studies
• Proficiency in the use of office suites and good statistical programming skills (SAS and R as a minimum)
• Good knowledge on regulatory standards (ICH, FDA, EMA, ENCEPP, HAS…)
• Proficiency in French and English
• Autonomy, organization skills, and ability to identify priorities
• Aspiration for excellence and performance
• Team spirit

Missions

• Writing and critical reviewing of study documentation on statistics (methodology, sample size calculations, statistical analysis plan, analysis methods, interpretation …)
• Implementation (programming) of relevant and well adapted statistical analyses
• Deliverables of the studies ensuring quality standards and timelines
• Participating on discussions concerning orientation of future projects, valorization of results …
• Writing/participation in the drafting of standard or specific operating procedures related to statistics
• Continuous development of personal statistical skills to keep up to date with scientific progress

Salary according to skills and experience.