Ardent Health runs clinical data management for late-phase trials across Belgium and the Netherlands. We are hiring a Clinical Research Associate to join the Clinical team.
You will monitor a portfolio of trial sites, on site and remotely, making sure each one follows the protocol and protects its patients. Expect regular travel within the region.
This role is based on site in Leuven. It is a full-time, permanent position. The pay range for this role is €43,000–€56,000 per year.
This is a fictional posting on the Jobo sandbox. Applications are never sent to a real employer.
What you'll do
- Monitor trial sites on site and remotely.
- Verify source data and chase open queries to closure.
- Train site staff on protocol amendments as they land.
- Check informed consent and safety reporting.
- Write clear, timely monitoring visit reports.
- Escalate quality issues early to the study lead.
Qualifications
Must have
- Bachelor's in Life Sciences, Pharmacy, Nursing or a related field
- ICH-GCP
- Site monitoring
- Source data verification
- Relationship building
Nice to have
- Oncology trials
- Risk-based monitoring
- Resilience
Benefits
- Meal vouchers and eco-cheques
- 32 days of annual leave
- Company car or mobility budget
- Net expense allowance
- Mental health support through a confidential service