EXPERIENCED CLINICAL RESEARCH ASSOCIATE
Description:
- Organisation, coordination and management of clinical trials;
- Monitoring research centres for verification and quality control;
- Support in writing of study documents (protocol, CRF, ...).
Profile:
- At Least 18 months experience as CRA;
- Good knowledge of ICH/GCP and other regulations;
- Scientific or (para)medical background;
- Good knowledge of Dutch, French and English;
- Willing to travel within the Benelux;
- Possession of driver licence B;
- Well organized, positive thinking person who can work independently;
- Flexible and communicative person.
We offer:
- attractive working environment that stimulates creativity and personal initiative;
- Result driven, dynamic team;
- Attention for training;
- competitive salary and extra-legal package;
- Company car;
- Possibility for home work
If you are interested, for this challenging opportunity, you should apply in writing and enclose a copy of your curriculum vitae to AML Clinical Services, Anne-Mie Lenaers, Tempelzicht 8, B-3210 Linden (alenaers@aml-research.be).
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