Clinical Research Associate I

CRA I, ICON Biotech, Paris, Office based with Flex.

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.

Clinical Research Associate I (CRA I) – Paris, France

As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

This role requires candidates to be based in the Paris area as it will be office based and and will require national travel.

What You Will Do

Your role will involve delivering clinical trial monitoring activities to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Working independently to coordinate activities related to study set-up and monitoring, while maintaining accurate study documentation and study status reports.
• Conducting monitoring visits in accordance with study protocols, ICH-GCP guidelines and applicable regulatory requirements.
• Running sponsor-generated queries efficiently and supporting timely issue resolution.
• Taking responsibility for study cost efficiency and contributing to the preparation and review of study documentation and feasibility assessments for new proposals.
• Developing and maintaining strong collaborative relationships with clinical investigators, site staff and key stakeholders.
• Ensuring patient safety, protocol compliance and data integrity throughout the study lifecycle.
• Supporting study delivery through effective site management and communication.

Your Profile

Required qualifications and experience:

• University degree in Medicine, Life Sciences, Pharmacy, Nursing or an equivalent scientific discipline.
• Minimum 1 year of independent clinical trial monitoring experience as a CRA.
• Experience conducting site monitoring visits and managing study sites independently.
• Knowledge of ICH-GCP guidelines and the ability to review and evaluate clinical data.
• Excellent written and verbal communication skills in English and French.
• Strong interpersonal skills with the ability to manage site relationships and resolve queries effectively.
• Strong organisational skills and attention to detail.
• Willingness to travel as required (approximately 60%).
• Residency in the Paris area.

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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits 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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply