iconplc - Remote work

Lead regulatory submissions (CTA/IND/MAA) for a global pharmaceutical sponsor in this home-based role in Australia. Leverage 6+ years of pharmaceutical regulatory affairs experience to provide strategic guidance and lead internal teams. Enjoy a competitive package with health insurance and a supp...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitiv...

Join ICON plc as a Clinical Research Associate II or Senior in São Paulo. You will conduct site monitoring visits, ensure protocol/GCP compliance, and contribute to trials in key therapeutic areas. This role requires a science degree, CRA experience, 70% travel, and advanced English. We offer com...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate in São Paulo. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure trial integrity. This role offers significant travel, competitive benefits, and a chance to shape the future o...

Join ICON plc as a Senior Clinical Associate in Warsaw. Support clinical trial management with a focus on inspection readiness and document management. Requires a Bachelor's degree and 2+ years of CTA experience in Pharma/CRO. We offer competitive benefits including health insurance and retiremen...

Join ICON plc as a Visualization Developer and shape the future of clinical development. Leverage your 4+ years of experience with Python, Spotfire, and clinical data (SDTM) to build advanced analytics solutions. Enjoy a supportive, innovative environment with competitive health insurance and ret...