Clinical Research Associate II

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.

We are currently seeking a Clinical Research Associate II (CRA) to join our diverse and dynamic ICON Biotech team.

Our biotech division of 8,000 people operates with a mindset aligned to small and mid-sized biopharma. Our tailored teams and management understand the different pressures that are faced by Biotechs and will engage, collaborate and share ownership in the delivery of your clinical trials. 

This role requires residency in the Paris or Lyon areas and can be office-based (Hybrid) or remote.

What You Will Do:

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

• Independently monitor Phase II–IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements

• Managing clinical studies in France across multiple therapeutic areas including Oncology and innovative Biotech treatments.

• 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.

• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

• Manage study documentation, regulatory submissions, and ethics/IRB approvals

• Ensure study cost efficiency and timely issue resolution

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 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.

#LI-SC1
#LI-Hybrid

#LI-Remote

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