iconplc - Research and Development, Remote work

Join ICON as a Clinical Research Associate in São Paulo, Brazil. You will independently coordinate study setup and monitoring, ensuring ICH-GCP compliance and patient safety. We seek a science graduate with strong English communication skills and willingness to travel (60%). Enjoy competitive ben...

Senior Clinical Research Associate sought in Montreal, Toronto, or Ontario. Lead monitoring for clinical trials, ensuring GCP compliance and data integrity across multiple sites. Requires bilingual (French/English) expertise, 60% travel, and strong site management skills. Benefits include health ...

Join ICON as a home-based Clinical Research Associate in the UK. Leverage your ICH-GCP expertise and monitoring experience to oversee clinical trials, ensuring patient safety and data quality. This role requires a science degree, UK driving licence, and 40% travel to hospital sites. Enjoy flexibl...

ICON seeks a Global Study Manager (Clinical Trial Manager II) in Budapest, Hungary. You will design and analyze complex clinical trials, interpret medical data, and drive innovative therapies. Requires a Bachelor’s degree and 6-7 years of trial management experience, with strong regulatory knowle...

Senior Clinical Research Associate sought in Frankfurt, Germany, to lead site monitoring, ensure ICH-GCP compliance, and drive data integrity for innovative trials. Requires 2+ years CRA experience, a scientific degree, and 60% travel. Join ICON’s dynamic team to advance therapies while enjoying ...

Senior Clinical Research Associate sought by ICON Plc to lead vaccine studies in Frankfurt, Germany. This role demands 10+ months of CRA experience, fluency in German and English, and 60% travel for site monitoring. You will ensure GCP compliance, manage multiple sites, and drive data integrity. ...

Senior Clinical Research Associate sought by ICON Plc to oversee global trial activities in Kansas City, MO. Requires advanced life sciences degree, extensive CRA experience, and 60% travel. Manage multiple sites, ensure GCP compliance, and drive data integrity. Benefits include health insurance,...

Seeking an experienced Clinical Trial Manager to lead oncology studies from Seoul, South Korea, in a home-based role with ICON Strategic Solutions. You will drive clinical deliverables, manage cross-functional teams, and ensure regulatory compliance. Requires 2+ years of CTM experience in a globa...

Seeking a skilled Clinical Research Associate II for a home-based role in South Korea with ICON. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring and ensure data integrity. This role requires 60% travel and offers a dynamic environment advancing clinical develo...

Join ICON plc as a Site Management Associate I in Buenos Aires, Argentina. Support clinical trial sites by ensuring protocol compliance and GCP adherence. Ideal for candidates with a life sciences degree and strong organizational skills. Enjoy benefits like health insurance, retirement planning, ...

Senior Clinical Research Associate sought for global trials in Sydney, Melbourne, Brisbane, or Adelaide. Requires a Pharmacy degree, 4+ years monitoring experience with strong Oncology and Haematology focus, and ICH-GCP expertise. Manage full site lifecycle from initiation to close-out, ensuring ...

Join ICON plc as a Clinical Research Associate I or II in São Paulo, Brazil. This sponsor-dedicated role requires a university degree in science or medicine, ICH-GCP knowledge, and strong English communication skills. You will independently coordinate study setup and monitoring, manage sponsor qu...