Description
We are seeking a CRA II or Senior CRA to work remotely from Belgium, with approximately 8 days of on-site travel per month. As a CRA, you will play a critical role in ensuring the quality and integrity of clinical trials.
Job Summary: ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. We are a values-driven organisation, with integrity, collaboration, agility, and inclusion at the heart of how we work and interact with each other, customers, patients, and suppliers.
Responsibilities:
- Monitor sites independently, from selection to close-out
- Handle regulatory submissions and essential documents (ANSM, CPP)
- Review clinical trial data and resolve data queries in a timely manner
- Protect data quality, ensure protocol compliance, and safeguard patient safety
- Build strong relationships with investigators and site teams
Requirements:
- Master's degree in life sciences, pharmacy, or medicine, or a nursing qualification
- CRA II: 2+ years of independent monitoring; Senior: 4+ years
- Strong ICH-GCP and French regulatory knowledge
- Excellent communication skills in Dutch, English, and French
Benefits:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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