Senior Clinical Research Associate - Belgium

Medpace; Belgique; Hybrid; EUR 52,000 - 75,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Paid time off (PTO)

WFH flexibility after training

Job summary

Medpace is seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. The role focuses on site visits, source data verification, regulatory document review, and SAE reporting within a dynamic CRO environment.

The candidate will manage drug inventories, monitor patient recruitment, and collaborate with cross-functional teams to ensure compliant clinical development across trials.

Qualifications

• Bachelor of Science in health-related field is required.
• Previous CRA experience is required.
• Fluent in Dutch, English and French; strong communication skills.

Responsibilities

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites.
• Perform source document verification and case report form review.
• Perform regulatory document review.
• Conduct study drug inventory.
• Perform adverse event and serious adverse event reporting and follow-up.
• Assess patient recruitment and retention.

Skills

Medical terminology

Clinical patient management

Drug therapy basics

Clinical research methodologies

Dutch English French language skills

Education

Bachelor of Science in health-related field

Job description

Medpace is seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. The role focuses on site visits, source data verification, regulatory document review, and SAE reporting within a dynamic CRO environment.

The candidate will manage drug inventories, monitor patient recruitment, and collaborate with cross-functional teams to ensure compliant clinical development across trials.