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UK
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EuropeAbout the role
You will keep clinical studies running smoothly: scheduling participants, collecting data, maintaining study files and liaising with sponsors. This is a 12-month contract with a good chance of extension.
What you will do
- Schedule and support participant visits
- Enter and check study data
- Maintain study files and regulatory documents
- Liaise with sponsors, monitors and ethics committees
What you bring
- Degree in life sciences, nursing or a related field
- 2 or more years of clinical research experience
- Knowledge of Good Clinical Practice (GCP)
- Good English; German is a plus
- Right to work in Austria
About the employer
A university hospital research unit in Vienna. The employer's name is shared once you speak with your recruiter and agree to be put forward.