iconplc - France

Join ICON as a Clinical Research Associate in Paris. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy competitive benefits including health insurance, retirement planning, and global employee suppo...

Senior CRA opportunity with ICON Plc, homebased in the Paris area. Seeking an experienced professional with 5+ years of interventional study monitoring and extensive oncology expertise. Manage multiple sites, ensure GCP compliance, and travel nationwide 6-7 times monthly. Enjoy competitive benefi...

Lead Clinical Quality Compliance in Paris with ICON, a world-leading healthcare intelligence organization. You will manage compliance programs, oversee audits, and implement QMS to ensure regulatory alignment. Ideal for experts with a Bachelor's degree and proven experience in quality assurance w...

Senior Clinical Research Associate (CRA) with oncology experience needed in Paris, France. Join ICON, a world-leading clinical research organization, to manage sites independently while ensuring ICH GCP and French regulatory compliance. Requires 4+ years of monitoring experience, fluency in Frenc...

Join ICON plc as a Clinical Research Associate II in Paris, France. This FSP role offers hybrid or home-based flexibility with a top-tier global pharmaceutical partner. You will independently monitor Phase II–IV trials across Neurology, Rare Disease, Dermatology, and Oncology. Requires 2-3 years ...

Senior Clinical Research Associate sought for ICON’s FSP division in Paris. This hybrid or home-based role offers a productivity bonus and excellent benefits while managing Phase II–IV trials for a top French pharmaceutical leader. Requires fluency in French, 4+ years of independent monitoring, a...

Senior Clinical Research Associate sought by ICON plc in Paris, France. This role involves overseeing global clinical trials, ensuring GCP compliance, data integrity, and patient safety. Requires extensive CRA experience, strong site management skills, and 60% travel. Join a world-leading healthc...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in France. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, Phase I Oncology expertise, and 60% travel. We offer ...

Join ICON plc as a Study Start-Up Associate and help shape the future of clinical development from home in France. You will facilitate clinical trial initiation, ensure regulatory compliance, and support document preparation. This role requires strong organizational skills and offers competitive ...

Join ICON Plc as a Senior Clinical Research Associate (CRA) in Paris. Oversee clinical trial sites, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...