iconplc

Join ICON's dynamic team as a Study Start-Up Associate II, based in Seoul. You will lead clinical trial initiation, ensuring regulatory compliance with ICH-GCP and local requirements. This home-based role offers competitive health insurance and retirement benefits. Utilize your 2+ years of study ...

Join ICON plc as a Senior Clinical Research Associate in Lima, Peru. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise across multiple sites. This role offers competitive benefits and ...

Join ICON plc as a Senior Clinical Trial Assistant in Blue Bell, US. Utilize your life sciences background and extensive trial support experience to manage key administrative and operational tasks. You will ensure regulatory compliance and smooth study execution within a global leader. We offer c...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in Madrid or Barcelona. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, strong site management skills, and 60% t...

Join ICON plc as a Senior Study Start Up Associate in São Paulo. Drive clinical trial initiation through site feasibility, contracts, and regulatory submissions. Leverage your medical/science background and fluency in Portuguese/English. Enjoy competitive health insurance, retirement planning, an...

Join ICON plc as a Clinical Trial Assistant (CTA) in a hybrid role based in Sofia, Bulgaria. You will support clinical trial design, analysis, and document management using systems like eTMF. This role requires a scientific degree, trial process knowledge, and strong organizational skills. We off...