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Experienced Clinical Research Associate (CRA) - Belgium  

Company managed [?] Still accepting applications
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Posted on : 16 November 2016

Project Description

In our company, the CRA position is a challenging job. You will be involved in various projects of different clients and are responsible from the very start of the project till the end.  The CRA function focuses on all aspects required to initiate, maintain and close-out clinical trials including  feasibility assessments, developing study documents, submission to Ethics Committees and Regulatory Authorities.

Why are we different:
 
  • You will have ownership of the projects.
  • We are a small sized CRO with a family feel.
  • We value initiative and encourage your growth through continuous development.
  • We support you to find a balance between your professional and personal lives. 

What do you offer:
 
  • Master’s degree in a scientific or (para)medical discipline
  • Minimum 2- 3 year of monitoring experience in clinical research in Belgium and/or The Netherlands
  • Professional proficiency in Dutch, French and English
  • Good knowledge of international guidelines ICH-GCP  & relevant local regulations
  • Willing and able to travel in Benelux
  • Good analytical and problem solving skills
  • Ability to prioritize and manage multiple tasks
  • Team player and flexible 

What we offer :
 
  • A permanent position
  • Minimum 0,8 FTE
  • An attractive salary package, including daily allowance, company car, hospitalization insurance and group insurance
  • Possibility to work home-based (1-2 days per week)
  • Flexible working environment.