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Clinical Research Associate (BE)

12.12.2018 REF: O180147 Flemish Brabant

Organization

CRO

Description of the Position

Responsibilities:

* Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
* Perform source document verification and case report form review;
* Perform regulatory document review;
* Conduct study drug inventory;
* Perform adverse event and serious adverse event reporting and follow-up; and
* Assess patient recruitment and retention.

Demands of the Position

Qualifications:

* Bachelor of Science in health-related field;
* Previous experience as a CRA; with 2 – 8 years of experience
* Broad knowledge of medical terminology and clinical patient management;
* Basic knowledge of drug therapy techniques and clinical research methodologies;
* Broad knowledge of the local language (Dutch and French) and excellent English;
* Clinical research experience preferred.

Terms of Employment

Directly at the clients headcount.
Interested in this challenge and want to apply directly?! Please use the apply button below. For more information, feel free to contact Nick Dufour at 0032 (0)475 87 02 36 or n.dufour@theclinicalcompany.com.

Nick for Belgium

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+32 475 87 02 36n.dufour@theclinicalcompany.com

Simone for the Netherlands

Didn’t find the right job on our website yet? Interested in an introduction of our company and what we can do to your career? Please feel free to contact me!

+316 12996359simone.polman@theclinicalcompany.com

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