iconplc - Remote work

Join ICON plc in Seoul as a Study Start Up Associate II and help shape the future of clinical development. You will lead clinical trial initiation, ensure regulatory compliance, and manage essential documents. This role requires 2+ years of study start-up experience and offers competitive health ...

Join ICON plc as a Clinical Research Associate in Miami, focusing on start-up activities across multiple therapeutic areas. You will identify and activate trial sites, ensuring compliance with ICH-GCP. This role requires 2-3 years of monitoring experience and offers competitive health insurance a...

Advance your career as a Senior Clinical Research Associate with a global CRO leader. Utilize your oncology monitoring experience and ICH-GCP knowledge to drive clinical trials across Australia. This role offers significant travel, competitive benefits, and a chance to shape the future of clinica...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role from Madrid. You will oversee clinical trial sites, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and a willingness to tr...

Join ICON plc as a Senior Clinical Research Associate in Burlington, Canada. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires oncology monitoring experience and 60% travel. Enjoy health insurance, competitive retirement plans, and a supp...

Join ICON plc as a Clinical Research Associate in New Jersey. You will conduct on-site monitoring visits across the southeast, ensuring ICH-GCP compliance across key therapeutic areas like Oncology. This role requires 2+ years of monitoring experience and offers competitive benefits with up to 50...

Join ICON plc as a Senior Clinical Research Associate in Buenos Aires. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retir...

Join ICON plc, a global clinical research leader, as a Senior Clinical Trial Manager in São Paulo. You will ensure successful study delivery, managing budgets, monitoring plans, and enrollment for complex trials. This role requires 10+ years of experience and offers competitive health insurance a...

Join ICON plc as a Clinical Research Associate II in a home-based role from Madrid. 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 o...

Join ICON plc as a Pharmacometrician and shape the future of clinical development. Utilize your expertise in NONMEM/Monolix to drive regulatory strategy and analysis plans. This role requires a PhD and 3+ years of applied model-based drug development experience. Enjoy competitive benefits includi...

Join ICON plc in Warsaw as a Local Trial Manager. Oversee the planning and execution of clinical trials, ensuring compliance with timelines, budgets, and regulations. Leverage your scientific degree and therapeutic expertise to lead cross-functional teams and manage site relationships. This role ...

Join ICON plc as a Clinical Research Associate II in Reading. You will conduct site monitoring visits, ensure ICH-GCP compliance, and contribute to innovative clinical trials. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive benefit...