iconplc

Senior Clinical Research Associate sought by ICON Plc to oversee clinical trials in Warsaw or Gdansk, Poland. This role demands a Bachelor's in a scientific field, extensive CRA experience, and expertise in site management, GCP, and regulatory compliance. You will monitor sites, ensure data integ...

Senior CRA opportunity at ICON plc, a world-leading clinical research organization. Based in Warsaw or Gdansk, Poland, this role involves overseeing clinical trials, ensuring GCP and regulatory compliance, and managing multiple sites. Requires a Bachelor's in a scientific field, extensive CRA exp...

Seeking an experienced **CRA II** in **Hangzhou, China** to conduct site monitoring and ensure ICH-GCP compliance. Requires a Bachelor's in science/healthcare and 2+ years of clinical research experience. Enjoy competitive benefits including health insurance, retirement planning, and flexible per...

Seeking an experienced **CRA II** in **Seoul, South Korea** to conduct site monitoring and ensure ICH-GCP compliance. Requires a Bachelor's in science/healthcare and 2+ years of clinical research experience. Enjoy competitive benefits including health insurance, retirement plans, and flexible per...

Join ICON plc as a CRA II in Seoul, South Korea, specializing in Oncology and Non-Oncology trials. Leverage 2+ years of clinical research experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, ret...

Senior Clinical Research Associate (Oncology) – Home-Based, Seoul, South Korea. Join ICON Strategic Solutions to lead global oncology SIT monitoring, ensuring GCP compliance and data integrity across multiple sites. Requires extensive CRA experience, strong site management skills, and 60% travel....

Join ICON plc as a CRA II or Senior CRA in a home-based role across the U.S. (Portland, Salt Lake City, Houston, Downers Grove, Lawrence). You will independently monitor clinical trials, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree, 1-3+ years of monitorin...

Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...

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 ...