iconplc - IT - Administration

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...

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 plc in Sydney as a Clinical Site Associate / Clinical Trial Associate. Support site activation, essential document management, and CRA coordination in a hybrid office-based role. Ideal for candidates with a life sciences degree and initial clinical research experience. Enjoy benefits li...

Join ICON as a Clinical Research Associate I in the United States. You will coordinate study setup, monitoring, and documentation while ensuring ICH-GCP compliance and patient safety. Requires a science degree, strong English communication, and 60% travel. Enjoy competitive benefits including hea...

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 ...

ICON plc seeks a Country Lead Monitor in Raleigh, NC, to drive clinical trial operations. You will manage study deliverables, ensure regulatory compliance, and build stakeholder relationships. Requires a science degree, therapeutic expertise, and prior monitoring experience. Enjoy competitive ben...

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...

Join ICON as a Site Management Associate I in São Paulo, Brazil. Support clinical trial site monitoring, ensure GCP compliance, and manage documentation. Ideal for candidates with a Bachelor’s in life sciences or clinical research and strong organizational skills. Enjoy benefits like annual leave...

Lead and coordinate clinical trial projects as a Trial Delivery Manager at ICON in Blue Bell, PA. We seek a seasoned project management professional with a Bachelor’s degree and proven leadership skills to deliver results on time and within budget. Drive cross-functional teams, manage stakeholder...

Join ICON plc as a Contract Associate in Madrid, Spain. Leverage your 2+ years of contract management experience and law/business degree to draft, negotiate, and manage agreements in a world-leading clinical research organization. Enjoy home-based flexibility, comprehensive health insurance, reti...