Senior Clinical Research Associate
Aussicht: 175
Update Tag: 16-11-2025
Kategorie: Planung / Projekte Wissenschaft R & D
Industrie: Research Services Biotechnology Research Pharmaceutical Manufacturing
Position: Mid-Senior level
Jobtyp: Full-time
Jobinhalt
As a Senior CRA 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 Senior CRA at ICON plc we expect you to have:
- about 4 to 6 years of experience in clinical trial monitoring
- a very good professional knowledge of Dutch andEnglish
- 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 one single 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 be supported by our ICON plc Operations 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
Frist: 31-12-2025
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