iconplc

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

Join ICON plc as a Clinical Research Associate II in Barcelona or Madrid. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitiv...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Romania. This remote, client-dedicated role involves monitoring Phase I-IV trials across therapeutic areas, requiring 3.5+ years of independent monitoring experience and 60% travel. We offer competitive b...

Join ICON plc in Madrid 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 health insurance, competitive reti...

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

Join ICON plc as a Senior CRA/CRA II in Belém do Pará. Design and analyze clinical trials, ensuring protocol compliance and data integrity. We require a Bachelor's degree, solid CRA experience, and ICH-GCP knowledge. Enjoy competitive benefits including health insurance and flexible offerings.

Join ICON plc as a Senior Clinical Research Associate or CRA II in the United States. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 1-3+ years of independent monitoring experience, ICH-GCP knowledge, and 60% travel. We offer compe...

Join ICON plc as a Clinical Research Coordinator in Łódź. You will support clinical project execution, analyze data, and ensure operational success. We require a relevant degree, project experience, and strong analytical skills. Enjoy competitive benefits including health insurance and a global s...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate. Utilize your 2-3 years of monitoring experience across therapeutic areas to drive site start-up in Texas. You will ensure GCP compliance, build key site relationships, and support patient recruitment. This role of...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health i...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, expertise in GCP, and 60% travel. We offer competitive hea...