About the Role
We are looking for an experienced CRA III (or Senior CRA, depending on experience) to support a high-profile pre-approval neurovascular medical device trial across 11 hospitals/research sites in Belgium, France, and Ireland. This role involves frequent site monitoring, ensuring patient safety, regulatory compliance, and high-quality data collection.
Key Responsibilities
* Conduct site initiation, monitoring, and close-out visits.
* Oversee site compliance with study protocols, GCP, and regulations.
* Maintain Investigator Site Files and ensure accurate documentation.
* Support recruitment, retention, and site performance.
* Troubleshoot site issues and implement corrective actions.
* Collaborate with investigators, IRBs/ECs, vendors, and internal teams.
* Provide regular updates on site and trial progress.
What We’re Looking For
* Bachelor’s degree in Life Sciences (or equivalent).
* 4–6 years of on-site monitoring experience (medical device preferred).
* Background in neurovascular or cardiovascular trials is a plus.
* Proficiency in English, Dutch, and French (working level – full fluency not required).
* Strong organizational and communication skills.
* Proficiency with Microsoft Office tools.
* Willingness to travel extensively across BE/FR/IE (monitoring visits every 1–2 months).