Experienced Clinical Research Associate, Multi-Sponsor Large Pharma
ICON
ICON seeks an experienced Clinical Research Associate (CRA II or Senior) to independently monitor multi-sponsor clinical trials across oncology, neurology, cardiology, gastroenterology, rare diseases, and ophthalmology. Based in Belgium with remote flexibility, the role involves site selection through close-out, regulatory submissions, data quality oversight, and investigator relationship management.
Responsibilities
- Independently monitor clinical trial sites from selection through close-out activities
- Prepare and handle regulatory submissions and essential documents with French authorities
- Review trial data and resolve data queries with timely follow-up
- Ensure protocol compliance, data quality standards, and patient safety protections
- Develop and maintain strong relationships with site investigators and teams
Requirements
- Master's degree in life sciences, pharmacy, medicine, or nursing qualification
- CRA II: 2+ years independent monitoring experience; Senior: 4+ years
- Strong ICH-GCP and French regulatory knowledge (ANSM, CPP)
- Fluency in Dutch, English, and French
- Ability to travel approximately 8 days per month on site
L'offre d'emploi a été publiée il y a 6 jours
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