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.

The role is open to CRA II and Senior CRA levels, with responsibilities including:

• Monitoring sites independently, from selection to close-out
• Handling regulatory submissions and essential documents (ANSM, CPP)
• Protecting data quality, protocol compliance and patient safety
• Building strong relationships with investigators and site teams
• Mentoring junior CRAs (Senior level)

Requirements include:

• 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
• Fluent French and professional English

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development, which may include:

• 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

Job Data by YubHub.

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.

The successful candidate will work on global programmes for the world's leading pharmaceutical companies, collaborating with France's most established research sites. This is a stable organisation offering proven processes, long-term opportunities, and a clear career path for progression.

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
• Fluent French and professional English

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

Inclusion and Accessibility: ICON is an equal opportunity employer committed to building an inclusive and accessible workplace where everyone feels valued and supported.

Job Data by YubHub.