Clinical Research Associate II - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA · Zaventem, Belgium
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Role summary
IQVIA seeks an experienced Clinical Research Associate II to conduct site monitoring activities across clinical trials in Belgium within a sponsor-dedicated model. The role involves monitoring visits, protocol training, recruitment oversight, regulatory compliance management, and documentation while collaborating with study teams. Candidates require a scientific degree, 18+ months of CRA experience, and fluency in Dutch, French, and English.
What they're looking for
- University degree in scientific or healthcare discipline
- Minimum 18 months independent on-site monitoring experience as CRA
- Fluent in Dutch, French, and English (written and spoken)
- Knowledge of GCP and ICH guidelines with applied regulatory expertise
- Strong interpersonal and cross-cultural communication abilities
- Collaborative mindset for cross-functional team engagement
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities
- Develop and track subject recruitment plans with assigned sites to meet project goals
- Administer protocol training and establish ongoing communication with study sites
- Monitor study progress including regulatory submissions, enrollment, CRF completion, and data queries
- Maintain and organize trial documentation including TMF and ISF records per GCP requirements
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.