Clinical Research Associate II

☞ ICON plc

看过: 135

更新日: 16-11-2025

位置: Beerse Antwerp

类别: 规划/项目 科学 R & D

行业: Research Services Biotechnology Research Pharmaceutical Manufacturing

水平: Associate

工作类型: Full-time

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工作内容

As a CRA II you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently but always as part of the client and ICON plc team.

Since ICON plc is a world-leading healthcare intelligence and Clinical Research Organisation, our clients expect us to be an added value to their teams. Therefore, as a CRA II at ICON plc we expect you to have:

  • about 2 to 3 years of experience in clinical trial monitoringor similar experience in the industry
  • a very good professional knowledge of Dutch and English
  • a knowledge of French (B1 level)

What’s in it for you?

You will be part of an organisation that has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.

You will work in highly committed and professional teams at the client but also within ICON plc. Since you can work for onesingle sponsor you will have the opportunity to gain indepth experience. We take into account your background and personal interests and see in which team you will fit best. You will besupported byour ICON plcOperations Managers who will make sure that during your career at ICON plc you can develop in the best way.

You can balance your professional and private time as our clients expect you to be onsite for 1 or 2 days a week in an office of your choice.

We offer you a permanent contract with an extensive package of extra-legal benefits and a company car or car allowance.

Always at your disposal for additional information about our wonderful organisation.

Katrien

katrien.dooms@iconplc.com

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最后期限: 31-12-2025

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