Sr. Biostatistician M / F

buscojobs España; Badajoz; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Senior Biostatistician to join their dynamic team in the life sciences sector. This role involves collaborating with clinical researchers to develop statistical methodologies and analysis plans that directly impact clinical studies. You will have the opportunity to validate data, manage regulatory submissions, and contribute to innovative research tools. If you are passionate about making a difference in clinical research and thrive in a collaborative environment, this position offers a unique chance to shape the future of healthcare.

Formación

• Expertise in statistical methodologies and clinical study design.
• Experience in regulatory submissions to agencies like FDA and EMA.

Responsabilidades

• Develop statistical analysis plans and select appropriate models.
• Collaborate with clinical teams to ensure data consistency and integrity.

Conocimientos

Statistical Analysis

Clinical Research

Statistical Modeling

Data Validation

Regulatory Submissions

Educación

Master's in Biostatistics

PhD in Statistics

Herramientas

SAS

R

SPSS

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):

1. Participate in the development of working hypotheses in collaboration with physicians and the clinical studies team.
2. Select statistical models 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 local parameters.
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 technical exchanges with research team members.
14. Manage submissions to regulatory agencies such as the FDA and EMA.