Clinical Research Associate

About the Role

We are looking for an experienced CRA I/II (depending on experience) to support a high-profile pre-approval cardiovascular medical device. 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).
• On-site monitoring experience (medical device preferred).
• Background in neurovascular or cardiovascular trials is a plus.
• Strong organizational and communication skills.
• Proficiency with Microsoft Office tools.
• Willingness to travel extensively across BE.