As a Clinical Research Associate, you play an important role in clinical studies within the medical device sector. You guide study centers through the entire process, from initiation to close-out. You monitor data quality, patient safety, and compliance with laws and regulations. You work closely with researchers, clinical teams, and other stakeholders.
What you will do.
- Guide study centers from start-up to study close-out.
- Conduct monitoring visits according to protocol and GCP guidelines.
- Monitor data quality and patient safety during clinical studies.
- Support study centers with operational and documentation questions.
- Actively follow up on recruitment, retention, and study progress.
- Collaborate with researchers, suppliers, and internal project teams.
- Report findings and follow up on corrective actions.
Profile
You work in a structured manner, communicate clearly with various stakeholders, and maintain an overview when multiple studies are running simultaneously. Thanks to your proactive approach, you take responsibility and know how to correctly set priorities.
What they ask
- Bachelor's degree in Life Sciences, Biomedical Sciences, Nursing, or equivalent.
- At least 2 years of experience in clinical research.
- Experience with medical device monitoring is required.
- Good knowledge of GCP guidelines and clinical regulations.
- Fluent in Dutch and English.
Preferences.
- Knowledge of French is a plus.
How to apply
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