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You are responsible as a Clinical Trial Expert for het preparation and implementation of :
You oversee and coordinate the trials from A till Z (protocol, product/placebo production, initiation, evaluation, interim visits, compliance procedures,…). You realize the monitoring according to the ICH-GCP. Thereby you review the quality and integrity of the clinical data, you process the obtained data and write the abstracts / publications in collaboration with the principal researcher or the research team. You present the results to the Science, Marketing and the Sales Team or at a scientific congress.
Further, you support the Medical Affairs department by looking up literature and answering questions.
In this role you report to the Science Director.
You will have an interesting function in a dynamic, fast growing, successful and financially healthy company. You receive enough independence and have the opportunity to take initiatives and promote. In addition, you can count on an attractive salary package with additional fringe benefits.
If you have any questions about this vacancy, contact HR by email (email@example.com) or phone (059 29 50 30).