[Hiring] Experienced Clinical Research Associate @ICON plc

Role Description

As a CRA II or Senior CRA, you will:

• Monitor your 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

Qualifications

• 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 in Dutch, English, and French

Requirements

• Home based in Belgium
• Travel around 8 days on site per month

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
• Benefits may vary depending on role and location

Company Description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.

• Oncology (Solid Tumors & Hematology), Neurology, Cardiology, Gastroenterology, Rare Diseases, and Ophthalmology
• Phase II to Phase III
• Global programmes for the world's leading pharmaceutical companies
• Working with France's most established research sites
• Stable organisation offering proven processes, long-term opportunities, and a clear career path for progression