Clinical Research Associate I - Sponsor dedicated - Netherlands - Home based (m/w/d)
IQVIA · Amsterdam, Netherlands
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a Clinical Research Associate I to conduct site monitoring visits, manage study progress, and ensure regulatory compliance for clinical trials in the Netherlands. This home-based role focuses on sponsor-dedicated work with direct site engagement and career development opportunities.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline
- Minimum 6 months independent on-site monitoring experience in CRO or pharmaceutical setting
- Full professional fluency in Dutch (C1 level) and English with strong medical writing skills
- Knowledge of GCP and ICH guidelines and clinical research regulatory requirements
- Strong organizational and problem-solving abilities
- Exceptional interpersonal and cross-cultural communication skills
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out activities
- Develop, track, and implement subject recruitment plans with assigned sites
- Deliver protocol training and maintain ongoing communication with study sites
- Evaluate site compliance with protocol and regulatory standards, escalating quality issues
- Generate monitoring visit reports, track regulatory submissions, and manage CRF completion
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.