Freelance Clinical Research Associate

EPM Scientific are currently partnered Sponsor who are seeking a freelance Clinical Research Associate (CRA) to support an exciting project. See a short summary below:

Contract Conditions:

• Start Date: ASAP
• Contract: 1 FTE, 12-month contract (opportunity to extend)
• Medical Device Project - Neurovascular
• Location: Belgium (Remote)
• Languages: Dutch, French & English required
• Project: Medical Device, Neurovascular

Key Responsibilities:

• Monitor clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements
• Act as the primary point of contact for site staff, supporting site initiation, monitoring, and close-out activities
• Ensure timely and accurate documentation, data collection, and reporting in line with project timelines
• Collaborate with cross-functional teams including Clinical Project Managers, Medical Monitors, and Regulatory Affairs
• Contribute to risk-based monitoring strategies and support audit readiness

Requirements:

• Strong experience as a CRA (5+ years preferred)
• Solid understanding of ICH-GCP and relevant regulatory environments.
• Proven ability to work independently and manage multiple sites
• Excellent communication and organizational skills
• Must Speak Dutch, French, and English

If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.