Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)
IQVIA · Zaventem, Belgium
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Role summary
IQVIA seeks an experienced Senior Clinical Research Associate for its Belgium-based sponsor-dedicated model. The role involves conducting site monitoring visits, managing study progress, ensuring regulatory compliance with GCP and ICH guidelines, and coordinating with clinical teams. Candidates need a scientific or healthcare degree, minimum three years of CRA experience, and fluency in Dutch, French, and English.
What they're looking for
- University degree in scientific or healthcare discipline
- Minimum 3 years on-site monitoring experience as CRA in CRO or pharma
- Fluent in Dutch, French, and English (written and spoken)
- Knowledge of GCP and ICH guidelines with regulatory compliance skills
- Strong interpersonal and cross-cultural communication abilities
- Organizational and problem-solving skills
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and closeout activities
- Collaborate with sites on subject recruitment planning and tracking aligned with study needs
- Deliver protocol training to sites and maintain regular communication regarding expectations
- Assess quality and integrity of site practices and escalate regulatory compliance issues
- Track study progress including regulatory submissions, enrollment, CRF completion, and data queries
Privacy & handoff
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