We are looking for an experienced clinical research professional who is passionate about partnering with study sites, safeguarding study quality, and driving successful clinical trial execution.
Requirements
- Prior experience as a Clinical Research Associate, Clinical Site Manager, or a similar monitoring-focused role
- Educational background in Life Sciences (e.g., Biomedical Sciences, Pharmacy, Nursing, Biology, etc.)
- Solid understanding of GCP, ICH guidelines, and clinical trial operations
- Excellent communication and relationship-building skills
- Strong language skills in Dutch, French, and English (both written and verbal)
- Ability to work independently, show initiative, and take ownership of site performance
- Strong organizational skills and attention to detail
- Problem-solving mindset with the ability to address site-related challenges proactively
Benefits
- Various annual leave entitlements
- A range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
