Clinical Research Associate - Dutch Language Skills Essential
A fantastic opportunity for a CRA with at least 18 months experience to join this small privately owned company. A great atmosphere with a real team spirit. You will be based in the UK office in Berkshire but having the ability to speak Dutch is essential. Uk experience is not a requirement. Experience in study set up is also idea.
Key Responsibilities:
*Administration and full site responsibility for clinical studies according to company SOPs, ICH-GCP and local regulations.
*May act as mentor for less experienced CRAs.
*Ensures clinical trials are monitored such that subjects' rights, safety and well being
are protected and that the clinical trial data are reliable.
*Assists the Project managers in the perparation and review of protocols and informed consent forms.
*contributes to CRF design and clinical trial document develpments as they pertain to clinical monitoring activities.
Key Requirements:
Well established monitoring experience, either CRO or Pharmaceutical industry
Fluent Dutch/Flemish language is essential and excellent spoken/written English
Experience of Oncology or ITU trials is advantageous.
Graduate or equivalent, ideally in scientific or healthcare discipline.
KEY WORDS: Belgium Dutch Flemmish CRO Pharmaceutical Small Oncology ITU CRA Permanent South East UK
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