iconplc

Join ICON plc as a Clinical Associate (CTA) in Blue Bell, PA, and support cutting-edge clinical trials. Leverage your scientific degree and CRO experience to coordinate study activities, ensure regulatory compliance, and drive data accuracy. Enjoy competitive benefits including health insurance, ...

Join ICON as a Clinical Research Associate I in Buenos Aires. Leverage your CTA or clinical research experience and ICH-GCP knowledge to monitor studies, ensure patient safety, and manage sponsor queries. Enjoy extensive benefits including health insurance, retirement planning, and global employe...

Seeking an experienced **Project and Portfolio Manager** in **Blue Bell, PA** to lead large-scale programs and cross-functional teams. You will drive complex projects from planning to delivery, managing budgets, resources, and risk. Requires a Bachelor’s degree, proven program management success,...

Senior CRA opportunity in Montreal, Canada, with ICON Plc, specializing in Medical Device and Cardiology trials. You will oversee site monitoring, ensure GCP and regulatory compliance, and manage multiple projects. Requires a Bachelor’s in a scientific field, extensive CRA experience, and strong ...

Join ICON as a Clinical Research Associate in Chengdu, China. 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 emplo...

Join ICON as a Clinical Research Associate in São Paulo, Brazil. You will independently coordinate study setup and monitoring, ensuring ICH-GCP compliance and patient safety. We seek a science graduate with strong English communication skills and willingness to travel (60%). Enjoy competitive ben...

Senior Clinical Research Associate sought for a dynamic role at ICON, overseeing global trials with a focus on ophthalmology or gene therapy. Requires 5+ years of CRA experience, deep ICH-GCP knowledge, and 60% travel. Drive site management, ensure data integrity, and advance innovative treatment...

Join ICON as a Clinical Research Associate in São Paulo, Brazil. Leverage your ICH-GCP expertise to design, monitor, and analyze clinical trials, ensuring data integrity and patient safety. Requires a scientific degree, strong organizational skills, and 60% travel. Enjoy competitive benefits incl...

Join ICON as a Clinical Research Associate in Western Canada (Alberta, Vancouver, Burlington). Monitor Oncology studies in a sponsor-dedicated program, ensuring patient safety and regulatory compliance. Requires a science degree, ICH-GCP knowledge, and Oncology monitoring experience. Enjoy compet...

Senior Clinical Research Associate sought in Montreal, Toronto, or Ontario. Lead monitoring for clinical trials, ensuring GCP compliance and data integrity across multiple sites. Requires bilingual (French/English) expertise, 60% travel, and strong site management skills. Benefits include health ...

Join ICON as a Clinical Research Associate in São Paulo, Brazil. Leverage your ICH-GCP expertise and science degree to coordinate study setup, monitoring, and documentation. Ensure patient safety while managing sponsor queries and building strong site relationships. Enjoy benefits like health ins...

Join ICON as a Clinical Research Associate in São Paulo, Brazil. Leverage 2+ years of experience and ICH-GCP expertise to manage site monitoring, ensure protocol compliance, and drive data integrity. This role requires 60% travel and a valid driver’s license. Enjoy competitive benefits including ...