iconplc

Join ICON plc as a Laboratory Technician I in Whitesboro, NY. Perform manual testing, prepare reagents, and maintain quality control in the lab. This full-time role offers a competitive salary, annual bonus, comprehensive health benefits, and retirement plans. Contribute to shaping the future of ...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, re...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health in...

Join ICON plc as a Senior Clinical Research Associate in Seoul. Oversee global oncology trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Associate in Singapore. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires 2+ years of CRA monitoring experience, a relevant degree, and 60% travel readiness. We offer competitive health insurance, retire...

Join ICON plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive monitoring and site management expertise within a world-leading CRO. Enjoy competitive benefits...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Reading, UK. Support trial operations by ensuring site compliance, documentation accuracy, and audit readiness. This role requires a life sciences degree, strong organizational skills, and offers competitive benefit...

Join ICON plc as a Clinical Site Associate in Paris. Support clinical trial operations, ensure site compliance, and manage documentation in French and English. This office-based role offers a clear path to a travelling CRA position within a year, with comprehensive benefits.

Join ICON plc as a Clinical Research Associate II in Ankara. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement plans,...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II/Senior CRA in Belém do Pará. You will design trials, analyze complex medical data, and advance innovative therapies. We seek a degree holder with solid CRA experience in CRO/pharma and deep ICH-GCP knowledge. En...

Join ICON plc in Beijing as an Investigator Payments Coordinator. You will manage and process clinical trial investigator payments, ensuring accuracy and compliance. The role requires a finance/accounting degree, 2+ years' relevant experience, and strong organizational skills. We offer competitiv...

Join ICON plc as a Contract Analyst I in Beijing. Prepare and verify electronic invoicing, reconcile accounts, and manage client relationships for an assigned portfolio. This role requires a finance-related degree, strong analytical skills, and attention to detail. We offer competitive benefits i...