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.