Our client is a professional Clinical Research organization, based in Gelderland Netherlands.
A globally operating CRO that offers innovative solutions for clients in the pharmaceutical industry
As a CRA you play a fundamental role in our client’s drug development process.
Responsible for the successful management of investigator sites throughout the project, working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal SOP's.
Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at site.
Ensure integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.
Demonstrate experience of working in either a fully independent monitoring role, in-house monitoring role, or as a clinical research nurse
Working knowledge of ICH-GCP guidelines and local and international regulatory requirements
Fluent in English, a team player and effectively communication skills
Oncology experience is a huge plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Hanneke de Koning.
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