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Clinical Research Associate - Netherlands

We are currently looking for a Clinical Research Associate for an International CRO company based in the Netherlands. We need an passionate and flexible person to evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations and escalate quality issues to Clinical Team Lead (CTL) and/or line manager.

Main Duties-
* Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
* Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
* Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation.
* Provide assistance to more less experienced clinical staff.

In return my client offers a highly competitive remuneration and benefits including -
* Excellent holiday allowance
* Health care
* Excellent opportunities for progression

So if you hold a Degree, in a scientific or healthcare discipline complimented by solid prior monitoring experience and lead CRA responsibilities - please forward your CV to jody@stelfoxuk.com or call me on 01273 727930 for a more in depth discussion.