iconplc - IT - Administration, Remote work

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, ...

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 ...

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 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 ...

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...

Join ICON plc as a Clinical Pricing & Payments Senior Associate in Barcelona, Spain. Leverage 3+ years of financial support experience to create clinical study budgets and pricing proposals. You will develop fair market value guidelines and maintain pricing tools in a home-based role. Enjoy compe...

Senior Clinical Research Associate needed for Neurovascular trials in the Central/Midwest US. Monitor complex studies onsite or remotely, ensuring ICH-GCP and FDA compliance. Requires a BS in Life Sciences, 3+ years of CRO/pharma monitoring experience, and strong problem-solving skills. Enjoy com...

Senior Clinical Trial Manager (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...