Biostatistician - Strasbourg, France
CTC Clinical Trial Consulting - France

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Reference Number: 50-12-759-B-W-JW

Type of placement: Permanent

Location: Strasbourg, France

Main Responsibilities:
You will be responsible for all statistical aspects of a clinical trial:

Development of protocols

Statistical Analysis Plans

Review of data as well as statistical analyses with SAS

Quality control of the results

Statistical Reports / Sections of a clinical report

You will be integrated into project teams working in a wide variety of therapeutic areas and you will have the opportunity to develop your skills.

Qualifications and Experience:
With a higher education in Statistics (Master, PhD), you master essential SAS and justify an experience of at least 2 years gained in the field of clinical research (pharmaceutical or CRO).

Fluent in both written and spoken English

Relevant working/residency permit or EU-Citizenship required

Our offer:
A competitive salary

The possibility for development and advancement within a dynamic environment

The innovative and stimulating atmosphere of an international environment

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