Senior Clinical Research Associate

Senior Clinical Research Associate - Belgium

Chloe O'Shea is partnering with a leading global clinical research organization (CRO) recognized for delivering high-quality, patient-centric studies and investing in their teams. We are currently seeking an experienced Clinical Research Associate (CRA). This role offers a manageable workload of 6–8 site visits per month, allowing you to focus on thorough monitoring and building strong relationships with sites.

The Role

As a Clinical Research Associate, you will be responsible for overseeing clinical trial activities across Belgium. You will collaborate closely with investigative sites and sponsor teams to ensure trials are conducted in compliance with study protocols, ICH-GCP guidelines, and Belgian regulatory requirements. This position is suited for professionals who value quality, collaboration, and making a meaningful impact on research.

Key Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits throughout Belgium
• Ensure sites comply with ICH-GCP, Belgian regulations, and sponsor protocols
• Verify source documentation, oversee investigational product accountability, and maintain accurate records
• Identify and escalate issues proactively to support smooth study progress
• Build and maintain positive working relationships with site staff and sponsor teams
• Provide guidance and training to site personnel to ensure protocol adherence and data integrity
• Maintain trial documentation using CTMS, eTMF, and EDC systems

Requirements

What You Can Expect

If you’re an experienced CRA seeking a role that respects your expertise and offers stability alongside meaningful work, we’d welcome your application. Please get in touch for a confidential conversation or apply today.