Senior Clinical Research Associate - 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 Senior Clinical Research Associate for sponsor-dedicated clinical operations in the Netherlands. The role involves conducting site monitoring visits, managing study progress, ensuring regulatory compliance, and collaborating with global teams on clinical trials.
What they're looking for
- Bachelor's degree in scientific discipline or healthcare field
- Minimum 3 years independent on-site CRA monitoring experience in CRO or pharma
- Full professional fluency in Dutch (C1 level minimum) and English with medical writing skills
- Strong knowledge of GCP and ICH guidelines and clinical research regulations
- Exceptional interpersonal and cross-cultural communication abilities
- Organizational and problem-solving skills with collaborative mindset
What you'll be doing
- Conduct site monitoring visits including selection, initiation, monitoring, and close-out per protocol and regulatory requirements
- Work with sites to develop, drive, and track subject recruitment plans aligned with project needs
- Administer protocol training to sites and establish ongoing communication to manage expectations
- Monitor study progress by tracking regulatory submissions, enrollment, CRF completion, and data queries
- Create and maintain documentation including visit reports, follow-up letters, and study records
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.