Clinical study coordinator
Siège de l'AP-HP · Public hospitals
En français : Coordinatrice d'études cliniques
This job in plain words
You manage the steps for setting up and following clinical studies, working with medical and paramedical teams in the clinical departments. The job is based in Paris, in research.
Can you apply?
The page shows a pay range for contract staff, so contract workers can be hired. Other conditions are not stated.
- Diploma
- Bac +5 (master's level) in a scientific field
- Experience
- Ideally at least 6 months of experience
The profile they want:
- Master's degree (bac +5) in a scientific field.
- Good organisation and prioritisation skills.
- Knowledge of the Microsoft Office suite.
- Excellent attention to detail.
- Very good oral and written communication skills.
What you would do
- Manage and coordinate the steps of clinical studies.
- Work with medical and paramedical teams in the clinical departments.
- Check and monitor the quality of services.
- Coordinate programmes, projects and activities.
- Set up and build the document archiving plan.
- Lead one or more teams and manage their development.
How to apply
Apply on the employer's website, through the offer on Choisir le Service Public.
We wrote this summary automatically from the official offer. Only the offer published on Choisir le Service Public counts: read it before you apply. Source: Choisir le Service Public (DGAFP), Etalab 2.0 licence.
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