iconplc

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, a global clinical research leader, as a Clinical Trial Associate in Shanghai. Utilize your life sciences degree and clinical research experience to support trial design, implementation, and monitoring. You will ensure protocol adherence and data integrity while collaborating with c...

Join Accellacare, part of ICON's network, as a Sr Clinical Research Nurse in Hickory, US. Autonomously coordinate and conduct clinical trial procedures, ensuring protocol compliance and patient care. Requires an RN/LPN license and strong GCP knowledge. Enjoy competitive benefits including health ...

Lead site contract negotiations for clinical trials across Poland, Bulgaria, Czechia, Ireland, or Romania. This homebased or office role requires 3-6 years of site contracts experience and expertise in Clinical Trial Agreements. Drive study timelines, ensure compliance, and mentor a team within a...

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...