Clinical Research Associate – Belgium (Home-Based / Hybrid)
Chloe O'Shea is partnering with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking a Clinical Research Associate to join a dedicated single-sponsor team in Belgium. This is an exciting opportunity to take ownership of site responsibilities, strengthen your expertise, and accelerate your career in clinical research, all while enjoying the flexibility of a home-based or hybrid position.
The Role
As a CRA, you will be responsible for the successful management of clinical trial sites across Belgium. You will act as the primary point of contact for investigative sites, ensure compliance with study protocols, ICH-GCP, and local regulatory requirements, and manage all aspects of site monitoring. This role is ideal for CRAs who already have hands-on monitoring experience and are looking to further develop their career within a dedicated, supportive team.
Key Responsibilities
* Independently manage site qualification, initiation, monitoring, and close-out visits.
* Ensure strict compliance with ICH-GCP, local regulations, and sponsor SOPs.
* Conduct source data verification, investigational product accountability, and maintain accurate site documentation.
* Build and maintain strong professional relationships with site staff and study teams.
* Proactively identify, resolve, and escalate site-level challenges to keep studies on track.
* Maintain complete and accurate trial documentation in CTMS, eTMF, and EDC systems.
Requirements
* Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
* 6–18 months of independent monitoring experience (CRO or pharmaceutical company).
* Knowledge of ICH-GCP and Belgian clinical trial regulations.
* Fluent in English and French, with basic Dutch.
* Strong communication, organizational, and relationship-management skills.
* Based in Belgium, with flexibility for home-based or hybrid working.
What’s in It for You?
This role offers a competitive salary and benefits package, flexible working options, and the opportunity to take ownership of clinical trial sites while building a strong foundation for your clinical research career. You will gain experience working on meaningful studies, collaborate with an international team, and develop the expertise needed to progress quickly in the field.
If you are a CRA with hands-on monitoring experience looking to take on real responsibility and grow your career, we’d love to hear from you. Apply today to join a global team dedicated to advancing clinical research and making a tangible impact.