Clinical Trial Expert

Job Description

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.


  • You have a master degree in a paramedical field of study;
  • You have a good knowledge from and preferably an experience in the clinical research processes and the  coordination of clinical studies;
  • You have experience with monitoring;
  • You have knowledge of ICH-GCP and regulations related to clinical research;
  • You can communicate fluently in Dutch, French and English (orally and in writing);
  • You have good IT knowledge (Office applications and reference software);
  • Knowledge of statistics is an added value;
  • You have good presentation skills;
  • You can work both independently and in team;
  • You can easily set priorities;
  • You have a sense of responsibility;
  • You are interested in micronutrition and a healthy lifestyle.


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 ( or phone (059 29 50 30).