SSU Clinical Research Associate at IQVIA Belgium, responsible for site selection, initiation, monitoring, and close-out visits, ensuring compliance with regulatory requirements and SOPs.
Requirements
- Conduct site selection, initiation, monitoring, and close‐out visits
- Manage study start‐up activities up to site green light
- Ensure compliance with ICH‐GCP, regulatory requirements, and SOPs
- Track study progress (regulatory submissions, recruitment, data quality)
- Collaborate closely with investigative sites, clients, and internal teams
- Support seamless handover to execution CRAs
Benefits
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a stabile, international, reputable company
- Company car
- Mobile phone
- Attractive benefits packaging
