Functie omschrijving
In your first months, you’ll focus on:
Coordinating clinical trials in accordance with Good Clinical Practice and ISO 14155:2020, including trial monitoring ensuring high quality data Working closely with trial sites and principal investigators Designing clinical studies for technology development purposes together with the engineering team Analyzing and reporting clinical study results Supporting the reporting to the ethics committee and Notified Body Leading biomedical working students to perform study-related projects (such as data annotation) Other tasks including but not limited to providing demos to customers, supporting the engineering team with bench tests, literature research. This is what your success looks like: After 12 months you are the go-to person for coordinating clinical trials required for technology, regulatory and scientific purposes. You...