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
A competitive salary
The possibility for development and advancement within a dynamic environment
The innovative and stimulating atmosphere of an international environment
Jobwinner.ch - il y a 12 mois