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The company offers excellent training as well as personal and career development opportunities in this expanding company. Furthermore, careful selection of employees has ensured an open, friendly and fun working environment and the company enjoys a very low staff turnover rate.
Your tasks:
Planning, co-ordination and overviewing of all monitoring activities of clinical trials to ensure the highest quality, that time-frames are met, communication with the client etc. The trials will be conducted in Belgium and the Netherlands as part of international projects to GCP Company standards. It is also of extreme importance to handle submissions to the regulatory authorities in Belgium an/or The Netherlands:
Requirements:
*University life sciences degree or nursing qualification.
* Minimum of 3 years experience as a CRA working on Phase II to IV trials in at least one of the following indications: oncology, virology, immunology, transplantation medicine
* Fluency in French and/or Dutch, excellent English
* In depth knowledge of FDA and ICH GCP requirements
* Excellent communication skills and computer literacy
* Willingness to travel
* Willing to work homebased
Benefits:
My client offers the opportunity to work at the highest level in a respected international organisation. This is a permanent full time position with attractive salary and add-ons. Please note that a company car cannot be provided. Instead you will receive a company car allowance.
If you meet the specifications above and wish to apply for the positions, please attach your CV as a WORD document via the link given and do not forget to mention your notice period as well as your availability for a phone call from my side.
Contact Person:
Aleksandra Stojanovic, Principal Consultant Clin Ops
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