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Senior clinical research associate

Tournai
AL Solutions
Publiée le 24 juillet
Description de l'offre

Senior Clinical Research Associate - Belgium


Chloe O'Shea is proud to partner with a leading global CRO delivering cutting-edge solutions in clinical development. We are seeking an experienced Clinical Research Associate (CRA) to join a dynamic and dedicated team in Belgium for an exciting single-sponsor opportunity. This position offers a sustainable workload of 6–8 site visits per month, allowing you to focus on high-quality monitoring and meaningful site engagement.


The Role

As a Clinical Research Associate (CRA), you will play a vital role in overseeing the execution of clinical trials across Belgium. Collaborating closely with investigative sites and sponsor teams, you will ensure compliance with study protocols, ICH-GCP standards, and Belgian regulatory requirements. This is an ideal opportunity for professionals who are passionate about advancing global research in a supportive, innovation-driven environment.


Key Responsibilities

* Conduct site qualification, initiation, monitoring, and close-out visits across Belgium.
* Ensure clinical trial sites operate in compliance with ICH-GCP, Belgian regulatory guidelines (e.g. FAMHP requirements), and sponsor protocols.
* Verify source data, oversee investigational product accountability, and ensure accuracy and completeness of site documentation.
* Identify and escalate site-level issues proactively to support timely resolution and smooth study progress.
* Build strong, collaborative relationships with site staff and sponsor stakeholders.
* Provide training and ongoing support to site teams to ensure protocol compliance and data integrity.
* Maintain current and accurate documentation in systems including CTMS, eTMF, and EDC platforms.


Requirements

* Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related health field.
* At least 2 years of independent monitoring experience as a CRA in Belgium.
* Strong knowledge of ICH-GCP and Belgian clinical trial regulations.
* Fluent in Dutch and French, and English, both written and spoken.
* Excellent organizational, communication, and time-management skills.


What’s in It for You?

* Competitive salary and an attractive benefits package.
* Clear career growth pathways within a world-leading CRO.
* Flexible working conditions with reasonable travel expectations.
* Access to cutting-edge digital tools and global study networks.
* A culture that prioritizes work-life balance, mental well-being, and continuous learning.


If you’re an experienced and motivated CRA seeking to make a real impact in a high-performing and collaborative environment, we’d love to hear from you. Apply today to advance your clinical research career in Belgium!

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