iconplc - IT - Administration

ICON seeks a Clinical Research Associate I in Shanghai to design and monitor clinical trials, ensuring ICH-GCP compliance and data integrity. Ideal candidates hold a Bachelor's in science/healthcare with 1+ year CRA experience. This role involves site visits, protocol oversight, and collaboration...

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...

Senior CRA role in Warsaw, Poland. Seeking a Clinical Research Associate with 2+ years of experience, a scientific degree, and ICH-GCP expertise. Responsibilities include site monitoring, data integrity, and protocol compliance. Benefits include health insurance, retirement planning, and global e...

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...

Join ICON as a Clinical Research Associate I in Seoul, South Korea. Leverage your oncology experience and ICH-GCP expertise to independently coordinate study setup, monitoring, and documentation. This role requires 60% travel and strong communication skills to build collaborative relationships wi...

ICON seeks a Clinical Research Associate (CRA II) in Seoul, South Korea. You will design and analyze trials, ensure ICH-GCP compliance, and conduct site monitoring visits. Requires a scientific degree and 2+ years of CRA experience with strong organizational skills. Benefits include health insura...

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,...