Clinical Research Associate - Netherlands

Role:

Clinical research Assoc

A Clinical Research Associate is required for a leading healthcare company based in the Netherlands

Within this position you will be responsible for:

• Identifying, selecting, initiating, and closing out investigational sites for clinical studies (phase II - IV)
• Ensure all applicable regulations and principles of ICG-GCP are adhered to
• Working independently and proactively to coordinate all necessary activities required to set-up and monitor a study
• Managing sponsor generated queries efficiently and responsible for study cost effectiveness

 Ideally, you will be an experience CRA and have previous experience in Phase II - IV Clinical Trials

Experience and Qualification 

• Knowledge of ICG-GCP guidelines and expertise to review and evaluate medical data
• Fluent in English as well as the local language
• High computer literacy 
• Must be able to travel internationally and domestically at least 60% and should possess a valid driving license.

 For further information on this position or similar roles please contact me on 00353 1 614 6072 or Jenny.Navan@cpl.ie 

Tagwords: CRA, Clinical Research Organisation, Netherlands, Dutch, CRO, Phase II, Phase IV

Keywords:

CRA |   Clinical Research Organisation |   Netherlands |   Dutch |   CRO |   Phase II |   Phase IV |