Clinical Research Associate II

CRA II , FSP Model , Paris Hybrid or Home Based. Productivity Bonus and Good benefits.

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

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.

We are currently seeking a Clinical Research Associate II (CRA II) to join our fast-paced, collaborative team within our Functional Service Provider (FSP) division.

In this role, you’ll be dedicated to a prestigious, top-tier global pharmaceutical partner headquartered in France, acting as a fully integrated member of their clinical operations team on high-impact global studies.

This role requires residency in the Paris area and can be office or home based.

What You Will Be Doing:

You will perform clinical trial monitoring tasks with a focus on technical quality, data integrity, and continuous improvement.

Key responsibilities include:

• Independently monitor Phase II–IV clinical trials as a dedicated resource to a major French pharmaceutical leader, ensuring full compliance with ICH-GCP and specific sponsor SOPs.
• Manage clinical studies in France across multiple therapeutic areas including Neurology, Rare Disease, Dermatology, and Oncology.
• Conduct site qualification, initiation, monitoring, and close-out visits, ensuring the highest standards of site performance and protocol adherence.
• Build and maintain strong relationships with investigators and site personnel to drive recruitment and facilitate smooth trial operations within this exclusive partnership.
• Perform data review and resolution of queries to maintain the highest quality of clinical data within the sponsor’s proprietary systems.
• Contribute to the preparation and review of study documentation, including monitoring plans and clinical study visit reports.
• Manage study documentation, regulatory submissions, and ethics/IRB approvals to ensure strict adherence to trial timelines.
• Support study cost efficiency and provide proactive resolution for site-level issues to meet critical milestones for our pharmaceutical partner.

Your Profile:

You will have a solid foundation in clinical trial monitoring and the ability to work independently within a sponsor-dedicated environment.

Required qualifications and experience:

• Bachelor’s or Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Minimum 2-3 years of experience as a Clinical Research Associate, with a proven track record of independent monitoring within a CRO or Pharma environment.
• Fluency in French and professional proficiency in English (mandatory for reporting and international stakeholder management).
• Strong knowledge of the French clinical trial landscape, local regulatory requirements, and ICH-GCP guidelines.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Excellent communication and interpersonal skills, with the ability to drive site compliance and represent a leading global sponsor effectively.
• Ability to travel as required to clinical sites and should possess a valid driver’s license.

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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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