Location
Paris
Posted
June 20, 2026
Commute
Local Area
Local Opportunity Near You!
This job is in your area. Enjoy a short commute and work close to home.
Job Description
CRA I Senior CRA I Clinical Monitoring
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre 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 world-class clinical research programme supporting a global pharmaceutical leader with an extensive and diverse therapeutic portfolio. We are looking for Clinical Research Associates at various levels who bring a minimum of 1 year of clinical monitoring experience within a pharma or CRO setting. Offering a flexible home-based working model, these opportunities are open to candidates across the Paris and Lyon regions, with more localised site allocations available for those based in Marseille.
As a Clinical Research Associate at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requir...
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre 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 world-class clinical research programme supporting a global pharmaceutical leader with an extensive and diverse therapeutic portfolio. We are looking for Clinical Research Associates at various levels who bring a minimum of 1 year of clinical monitoring experience within a pharma or CRO setting. Offering a flexible home-based working model, these opportunities are open to candidates across the Paris and Lyon regions, with more localised site allocations available for those based in Marseille.
As a Clinical Research Associate at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requir...