iconplc - Remote work

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...

Join ICON plc as a Senior Clinical Research Associate in Reading, UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insuran...

Join ICON plc as an Investigator Payment Associate in São Paulo. You will ensure accurate, compliant financial processing for global clinical trials. This role requires a finance/accounting background and knowledge of regulations like the Sunshine Act. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Lead Assistant and help shape the future of clinical development. This remote role requires strong organizational skills, fluency in English, and proficiency in Microsoft applications to provide key administrative support for clinical trials. We offer competit...

Lead global clinical trials from start-up to database lock as a Senior Clinical Trial Manager at ICON in Boston. Utilize your 10+ years of experience to oversee budgets, drive enrollment, and mentor CRAs. This pivotal role offers competitive health insurance, retirement planning, and a chance to ...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, re...