水平: Mid-Senior level

工作类型: Full-time

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工作内容

As a Trial Manager you will run assigned clinical trials. You will have operational oversight of assigned protocols from start-up through to database closure of the trial. You will be responsible for coordinating the local trial team to deliver quality data and trial documents that are aligned with SOPs, GCP and regulatory standards. The Trial Manager actively contributes to process improvement by training and mentoring of Clinical Trial Assistants and Clinical Research Associates.

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 Trial Manager at ICON plc we expect you to have:

  • More then 6 years of experience in clinical trial monitoring
  • 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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