CRA II

CRA II, Late Phase, Home-based, France. Candidates based in or near major metropolitan areas such as Paris, Lyon, Marseille, Toulouse, Bordeaux, Lille, Nantes or Strasbourg are preferred due to travel requirements.

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.

As a CRA within, Late Phase at ICON, you will play a key role in the delivery of Phase III, Phase IV and observational studies, ensuring clinical trials are conducted in accordance with the protocol, ICH-GCP, regulatory requirements, and ICON SOPs. You will work closely with investigative sites to maintain patient safety, data quality, and study timelines while contributing to the development of innovative therapies.

You will benefit from the scale, stability, and resources of a international CRO environment, while enjoying the career development opportunities, global reach, and collaborative culture that ICON is known for.

This role offers exposure to innovative clinical research programmes across multiple therapeutic areas, working alongside experienced study teams and some of the most established research sites in France.

What You Will Do

You will be responsible for the independent management and monitoring of assigned late phase clinical studies, including:

• Independently monitor Phase III + IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements
• Managing clinical studies in France across multiple therapeutic areas including Oncology, (solid tumor and hematology, Neurology, Psychiatry, Obesity, Cardiology and Dermatology.
• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.

Your Profile:

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements within a CRO or pharmaceutical industry environment.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Fluency in French and professional proficiency in English
• Strong organizational and communication skills, with attention to detail.

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What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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