Clinical Trial Associate

Clinical Trial Support I CTA I France

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

Join a global pharmaceutical innovator and contribute to life-changing clinical research

Step into a unique opportunity where you are fully embedded within a leading global pharmaceutical company based in the Paris region. Working side by side with industry experts, you will play a key role in advancing innovative therapies across high-impact areas such as oncology-hematology, neurology, and immunology. This position offers hands-on experience in a dynamic, international environment, where your work directly contributes to the development of cutting-edge treatments that improve patients’ lives worldwide.

As a Clinical Trial Associate at ICON, you will assist with the administration and coordination of clinical trials, and actively contribute to the advancement of innovative treatments and therapies.

What You Will Do:

Your role will involve delivering high-quality clinical research activities while collaborating closely with your team and key stakeholders in a fast-paced, science-driven environment.

Key responsibilities include:

• Assist in the coordination and administration of clinical trials, ensuring full compliance with study protocols and applicable regulatory requirements
• Maintain, track, and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
• Support the preparation and review of study-related materials, such as informed consent forms and case report forms
• Collaborate with cross-functional teams to ensure seamless communication and efficient trial execution
• Contribute to the tracking, analysis, and reporting of clinical trial metrics, timelines, and key milestones

Your Profile:

You bring a solid foundation in clinical research along with a strong drive to contribute to innovative healthcare solutions.

Required qualifications and experience:

• Bachelor’s degree in a scientific or healthcare-related field
• Initial experience or a strong interest in clinical research
• Good understanding of clinical trial processes, regulations, and guidelines
• Strong organizational skills with a high level of attention to detail
• Excellent communication skills and the ability to work effectively in a collaborative, fast-paced environment
• Proactive, adaptable, and solution-oriented mindset
• Willingness to travel as required (approximately 10%)

What ICON can offer you:

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.

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