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).