Reference: IdH 898971
Closing Date: 30 Nov 16
Salary (£): On Application
CRAs will typically be responsible for managing more investigational sites at any given time, depending upon the nature and complexity of the trial.
In this position you are responsible for setting-up, initiating and closing down investigational sites in the Netherlands. You are also responsible for monitoring and reporting on study progress of clinical trials in the Belgium and globally in accordance with established scientific, internal and Good Clinical Practice (GCP) guidelines in order to meet the research and commercial objectives of the company.
Duties & Responsibilities
The CRA will
Schipholweg 111, 2316 XC Leiden, Netherlands
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