![](https://www.radboudumc.nl/getmedia/72aed5a2-451c-478b-b675-a18a33984146/Clinical-Research-Unit.jpg?width=596&height=394&ext=.jpg&type=BlockColumn1Zoom1)
![](https://www.radboudumc.nl/getmedia/72aed5a2-451c-478b-b675-a18a33984146/Clinical-Research-Unit.jpg?width=596&height=394&ext=.jpg&type=BlockColumn2Zoom1)
About this team
We provide tailored support and execution in clinical research with patients and healthy volunteers.
read moreAbout this team
We provide practical researcher support for the initiation and/or conduct of clinical research (drugs/medical devices).
This involves studies ranging from phase 1 to 4, with patients and healthy volunteers. The responsibilities of our research nurses and assistants during a clinical study include logistics and planning of study visits, communication with the study participant/sponsor, nursing operations, sample processing in our lab, data management, and essential record keeping.
The research coordinator's support includes protocol writing, METC submission, local approval, budgeting, and financial administration. Our team is happy to provide customized services, jointly providing appropriate support in accordance with applicable laws and regulations.
De Clinical Research Unit is part of the research institute.
Our services for employees
Customized support
You can contact us for a specific service, or for complete support with the preparation, execution and completion of human-related research.
see page (intranet)Qualified staff
You can contact us if you are looking for a research coordinator, research nurse/local data manager and/or research assistant.
see page (intranet)Facilities
We provide research rooms and equipment needed to conduct clinical research according to applicable laws, regulations and policies.
see page (intranet)Additional services
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SUSAR reporting to the European Medicines Agency (EMA) where all studies at Radboudumc are the sponsor.
read more -
Room rental, with or without support service, is possible by arrangement.