iconplc

Seeking a Senior Clinical Site Manager (SCRA) for a rare, home-based, part-time FSP role (0.6 FTE) in Adelaide or Melbourne. Leverage your CRA II/Senior CRA expertise to build strong site relationships, drive patient recruitment, and ensure audit-ready studies for a leading biopharma. Enjoy flexi...

Join ICON as a Senior CRA in Montreal, Canada, and lead Oncology study monitoring in a sponsor-dedicated role. Leverage your ICH-GCP expertise and medical/science degree to ensure patient safety and data quality. Enjoy 60% travel, competitive benefits including health insurance and retirement pla...

Join ICON as a CRA II in Buenos Aires, Argentina, and drive clinical trial excellence. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Enjoy competitive benefits ...

Join ICON plc as a Clinical Site Associate in Frankfurt, Germany. Support site activation, essential document management, and CRA coordination for global clinical trials. Ideal for life sciences graduates with clinical research experience, strong organizational skills, and fluency in German and E...

Join ICON as a UK home-based Clinical Research Associate 1, specializing in In Vitro Diagnostics. This unique role offers a transition from lab-based work into clinical trial operations on a blue-chip diagnostics project. You will coordinate study initiation, monitoring, and completion while ensu...

Join ICON as a Clinical Site Associate in Milan, Italy. Support site management activities for clinical trials, working with CRAs and cross-functional teams on start-up, maintenance, and close-out. Ideal for candidates with a life sciences degree and initial clinical research experience. Enjoy be...

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...

Senior CRA, home-based in Poland. Join ICON, a world-leading clinical research organization, to oversee trial activities ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from flexible work, he...

Join ICON as a Clinical Research Associate II in Ho Chi Minh City, Vietnam. Leverage your 2+ years of CRA experience and ICH-GCP expertise to oversee site monitoring, ensure protocol compliance, and drive data integrity. This role offers extensive travel, competitive benefits including health ins...

ICON plc seeks a Clinical Research Associate II (XTA) in Chicago. Leverage 2+ years of on-site monitoring experience across multiple therapeutic areas. Ensure site compliance with ICH-GCP and manage visits using CTMS/eTMF. Enjoy competitive benefits, annual leave, and up to 50% travel across the ...

ICON plc seeks a Clinical Research Associate II in Seoul, South Korea. You will conduct Phase I-III oncology monitoring, ensuring ICH-GCP compliance and data integrity. Requires 2+ years of SIT onsite CRA experience and a scientific degree. Benefits include annual leave, health insurance, and ret...

Join ICON plc as a Clinical Research Associate in Montreal, Canada. Monitor multi-therapeutic area studies in a sponsor-dedicated program, focusing on Oncology. Leverage your ICH-GCP expertise and medical knowledge to ensure patient safety and data quality. Enjoy competitive benefits, including h...