Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)
Share role
The recipient sees their own assessment. Your profile and score are not shared.
About the role
Permanent, full-time remote Senior Clinical Research Associate role supporting clinical site monitoring, site management, recruitment and start-up activities across Brussels, Antwerp, Bruges and Liège. Requires 4–6 years of related experience, a bachelor’s degree or equivalent combination of education and experience, fluent written and verbal English, ICH-GCP knowledge, clinical systems proficiency and a valid driver’s license. French and Dutch fluency are stated in the title.
Key requirements
- • (Honors) Bachelor’s degree. Or an equivalent combination of education and experience may be considered.
- • At least 4 years of relevant experience
- • Required skills: Clinical site monitoring, Site management, Clinical trial start-up and site activation, Protocol and regulatory compliance, ICH-GCP, Investigational site liaison and issue resolution, Clinical supplies coordination, EDC systems, IRT, eTMF, CTMS, Microsoft Office Suite, Mentoring
- • Required language: English
- • Professional registration/licence (Belgium)
Opportunity details
- • Workplace: Remote
- • Employment: Permanent
- • Posted: Sep 17, 2026
- • Original advert language: English
Full vacancy
HealthRoleIQ regularly verifies this opportunity against the employer’s posting and highlights the details relevant to your match.
Employer’s role description
Job title: Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)
Department: Clinical Services
Team: Clinical Study Delivery - Monitoring & Site Management