Sr. Biostatistician M / F

buscojobs España; La Rioja; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An innovative company is seeking a Senior Biostatistician to play a crucial role in the development of statistical methodologies for clinical research. This position offers a unique opportunity to work in a collaborative international environment, directly impacting the future of life sciences. You will be responsible for creating statistical analysis plans, validating data consistency, and managing submissions to regulatory bodies. If you are passionate about advancing clinical research and thrive in a dynamic setting, this role is perfect for you.

Formación

• Expertise in statistical analysis and methodology for clinical studies.
• Experience in managing FDA and EMA submissions.

Responsabilidades

• Develop statistical models and methodologies for clinical research.
• Collaborate with clinical teams to ensure data consistency.

Conocimientos

Statistical Analysis

Clinical Research

Statistical Methodology

Data Management

FDA Submissions

Educación

Master's in Biostatistics

PhD in Statistics

Herramientas

SAS

R

Descripción del empleo

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) :

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

J-18808-Ljbffr