This is a permanent role offering wide exposure across the full study lifecycle, not just monitoring.
The Role
Responsibilities
As a CRA within this team, you will take responsibility for end-to-end site management activities across your assigned protocols. Typical responsibilities include:
- Contract negotiation and start-up activities
- Site initiation, routine monitoring and close-out
- Proactive issue resolution and relationship-building with sites
- Ownership of your protocols rather than operating in a bill-out model
- Approximately 6–8 visits monthly, managed flexibly
Experience Required
- Minimum 2+ years of independent onsite monitoring
- Biopharma therapeutic area experience; Cardiology exposure is ideal
- FSP experience beneficial
- Strong communication and site-facing skills
- Languages:Dutch and English required, French is a plus
- Remote across Belgium, with occasional travel to the Netherlands.
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