iconplc - Remote work

Lead US clinical trials as a Local Study Associate Director at ICON plc. This role requires 5+ years of US trial management experience and deep ICH-GCP knowledge. You will oversee study commitments, lead local teams, and ensure regulatory compliance. We offer competitive health insurance, retirem...

Join ICON plc as a Payment Analyst in Warsaw. Utilize your finance degree and 1-2 years' experience to ensure compliant investigator payments for clinical trials. You will process payments, resolve discrepancies, and streamline procedures in a dynamic, global environment. We offer competitive ben...

Lead our Business Continuity Management in Ireland. Develop and implement robust continuity strategies, conduct risk assessments, and lead recovery planning. This hands-on role requires a CBCP/MBCP certification, 5+ years' experience, and a willingness to travel. We offer competitive benefits inc...

Join a global pharmaceutical leader as a Site Investigational Product Specialist in Reading, UK. Utilize your extensive clinical trial and IP administration expertise (IV, SC, IM) in Oncology/Immunology. Ensure safe investigational product preparation and serve as the key liaison between sponsor ...

Join ICON plc as a Senior Clinical Research Associate in Mexico City. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% domestic travel. Enjoy competitive benefits including ...

Join ICON plc as a Clinical Research Associate II in Mexico City. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% domestic travel. We offer competiti...

Join ICON's AstraZeneca FSP program as a Global Clinical Trial Assistant. This home-based role requires 2+ years of global study support experience and ICH-GCP knowledge. You will manage the Trial Master File, coordinate study materials, and ensure regulatory compliance. We offer competitive heal...

Lead global clinical trials from Mexico City as a Senior Clinical Trial Manager with ICON. Utilize your 7+ years of CTM experience, including expertise in North America and LATAM studies, to oversee budgets, drive enrollment, and ensure study integrity. Enjoy competitive benefits while shaping th...

Join ICON plc as a Senior CRA or CRA in Blue Bell, USA. You will ensure protocol compliance and data integrity across clinical trial sites, requiring 1-3+ years of monitoring experience and ICH-GCP knowledge. This role involves ~60% travel and offers competitive health insurance, retirement plans...

Join ICON plc, a global clinical research leader, as a Senior CRA or CRA II in Blue Bell. Utilize your monitoring experience and ICH-GCP knowledge to ensure trial integrity and patient safety. This role offers significant travel, competitive benefits, and a chance to shape the future of healthcare.

Join ICON plc as a Clinical Research Associate in São Paulo. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel readiness. We offer health insurance, competitive retirement plans, ...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will design trials, analyze complex medical data, and ensure protocol compliance with ICH-GCP. This role requires a scientific degree, on-site monitoring experience, and 60% travel. We offer competitive health insurance and retir...