Ardent Health runs clinical data management for late-phase trials across Belgium and the Netherlands. We are hiring a Pharmacovigilance Associate to join the Drug Safety team.
You will process adverse event reports from intake to submission, working to strict timelines and an exacting standard. Training is thorough and the team is supportive.
This is a hybrid role based in Leuven, with two or three days a week in the office. It is a full-time, permanent position. The pay range for this role is €32,000–€41,000 per year.
This is a fictional posting on the Jobo sandbox. Applications are never sent to a real employer.
What you'll do
- Code events and products using MedDRA and WHO-Drug.
- Write clear case narratives.
- Meet regulatory reporting timelines.
- Support signal detection activities.
Qualifications
Must have
- Bachelor's in Life Sciences, Pharmacy, Nursing or a related field
- Case processing
- MedDRA coding
- Attention to detail
- Time management
Nice to have
- Argus Safety
- Medical writing
Benefits
- Meal vouchers and eco-cheques
- Group insurance and hospitalisation cover
- Company car or mobility budget
- Conference attendance budget