Clinical Research Associate (CRA) met eerste monitoring ervaring ()


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Actively looking for

Clinical Research Associates

with a minimum of 6 months monitoring experience for several companies

Job description:

The CRA is the go-between the investigator and the pharmaceutical company; ensuring that the clinical study is conducted according the guidelines. He/she is monitoring the collected data in the patients’ files and the medical records, informing the investigator of incorrect or missing data.

Overall organization, management and conduct of clinical trials by respecting all regulatory requirements and Good Clinical Practice:

Preparation & coordination of Clinical Trials:

– preparation of materials

– preparation of EC-submissions

– budget agreements with hospitals

– follow-up patient enrollment

– clinical trials monitoring

General administration related to clinical trials:

– clinical trials documentation management

– clinical trials invoices management

Regulatory issues:

– close follow-up of regulations

– SOP preparation & update

* General

– representative of the company

– monthly reporting to dividion management

Skills & personality:

* Scientific background

* Experience in clinical trials is mandatory

* Well-developed communication, presentation & computer skills

* Good administrative skills

* Good organizational skills

* High degree of independence

* Flexible

* Accurate, eye for detail

* FBeing fluent in Dutch, French & English is a requirement


Attractive salary package


Please send your English CV to [email protected]



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