Sr. Biostatistician M/F

TN France; France; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

An established industry player is seeking a Senior Biostatistician to join their dynamic team in France. In this role, you will leverage your expertise in statistical analysis and clinical research to shape the future of life sciences. You will work collaboratively with physicians and research teams, developing statistical methodologies and creating analysis plans that directly impact clinical studies. This is an exciting opportunity to contribute to innovative projects that improve patient outcomes while working in a supportive and international environment. If you are passionate about biostatistics and eager to make a difference, this position is perfect for you.

Qualifications

• Expertise in statistical analysis and methodology for clinical studies.
• Strong background in biostatistics and experience with FDA submissions.

Responsabilités

• Develop statistical methodologies and analysis plans for clinical trials.
• Collaborate with clinical teams to ensure data consistency and accuracy.

Connaissances

Statistical Analysis

Clinical Research

Statistical Modeling

Data Consistency Validation

Formation

Master's in Biostatistics

PhD in Statistics

Outils

SAS

R

Description du poste

You are a highly skilled professional with a passion for the world of life sciences and clinical research. You want to thrive in a dynamic and collaborative international environment where your expertise directly impacts people's lives. Come and join Aixial Group to contribute to shaping the future of clinical research!

We are currently looking for a Senior Biostatistician M/F to carry out the following tasks (non-exhaustive list):

1. Participate in the development of working hypotheses in collaboration with physicians and the clinical studies team.
2. Select a statistical model and define the statistical methodology for clinical studies.
3. Determine the number of subjects to be studied.
4. Create the statistical analysis plan.
5. Participate in protocol drafting and validation.
6. Set up randomization plans.
7. Validate data consistency in collaboration with the Data Management team.
8. Observe the consequences on the model of variations in a local parameter.
9. Perform and program analyses.
10. Write statistical sections of study reports.
11. Present statistical results.
12. Monitor and propose new statistical tools and methodologies through scientific and technical reading.
13. Participate in exchanges on technical subjects with members of the research team.
14. Manage submissions to the FDA (Food and Drug Administration) and EMA (European Medicines Agency).

Additional notes:

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