You are responsible as a Clinical Trial Expert for het preparation and implementation of :
- Clinical trials
- Observational trials
- Case studies
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.