iconplc - IT - Administration

Senior Clinical Research Associate needed for Neurovascular trials in the Central/Midwest US. Monitor complex studies onsite or remotely, ensuring ICH-GCP and FDA compliance. Requires a BS in Life Sciences, 3+ years of CRO/pharma monitoring experience, and strong problem-solving skills. Enjoy com...

Senior Clinical Trial Manager (Oncology) – Home-Based, Blue Bell, US. Lead end-to-end trial management as a site-aligned partner, driving communication and issue resolution. Requires 3-5+ years of trial management, solid tumor oncology expertise, and ICH-GCP knowledge. Enjoy competitive benefits,...

ICON plc seeks a Clinical Supplies Project Manager to join its world-leading clinical research team in Warsaw or Gdansk, Poland. You will manage global supply planning, forecasting, and IRT system setup for clinical trials. Ideal candidates bring 4+ years of clinical supply experience, strong pro...

Lead clinical trials as Director, Clinical Operations at ICON in Sofia, Warsaw, Belfast, Poland, or Ireland. Drive performance, ensure GCP compliance, and manage cross-functional teams to advance innovative therapies. Requires a life sciences degree and extensive CRO/pharma experience. Enjoy comp...

Join ICON as a Study Support Assistant in Warsaw, Poland, and play a key role in advancing clinical trials. We seek candidates with a high school diploma (Bachelor’s preferred) and administrative experience, ideally in healthcare. You will manage study documents, coordinate meetings, and ensure r...

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 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 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 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 ...

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...