iconplc - Research and Development, Hybrid work

Join ICON plc as a Clinical Research Associate II in Puerto Rico. 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...

Join ICON plc as a Clinical Site Associate in Milan, Italy. Support clinical trial operations by ensuring site compliance, documentation accuracy, and audit readiness. Requires a life sciences degree, clinical research experience, and fluency in Italian and English. Enjoy competitive benefits inc...

Join ICON plc in Mexico City as a Study Start-Up Associate II. Utilize your 2-4 years of clinical start-up experience and regulatory knowledge to support site activation and submissions. This role offers competitive benefits, including health insurance and retirement planning, in a global leader ...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Bangkok. You will ensure site compliance, manage documentation, and support audit readiness for clinical trials. This role requires a life sciences degree, strong organizational skills, and fluency in English. Enjoy...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Mechelen. Independently manage all trial site activities from start-up to close-out, ensuring protocol and SOP compliance. Enjoy a competitive package with health insurance and support programs, while making a real impact on global pa...

Join our team in Mexico City as a Regulatory Technician. You will manage clinical trial submissions using the CTIS system, ensuring compliance and quality. Ideal candidates have advanced English and 1-2 years in clinical research. We offer competitive health insurance and retirement plans.

Join ICON plc as a Senior Clinical Research Associate in Taipei. Oversee clinical trial activities, 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, r...

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...