iconplc - Remote work

Join ICON plc as a Clinical Research Associate I/II in São Paulo. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This sponsor-dedicated role requires a science/medicine degree, excellent English, and 60% travel readiness. Enjoy health insurance, competitiv...

Join ICON plc as a Senior Clinical Research Associate (CRA) and shape the future of clinical development. Oversee trial activities, ensure protocol/GCP compliance, and manage site performance across multiple projects. This role requires extensive CRA experience, strong monitoring skills, and 60% ...

Join the world's largest CRO as a Senior Clinical Research Associate in Montreal. Utilize your 2+ years of on-site monitoring experience and ICH-GCP expertise to conduct clinical trial site visits. This role requires up to 60% travel and offers competitive health insurance and retirement benefits.

Join ICON plc as a Senior Clinical Research Associate in Frankfurt/Mannheim. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy competitive benefits including health insu...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Kuala Lumpur. You will monitor sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel readin...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires 3+ years' CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement ...

Lead global cell therapy trials in Hematology/Oncology as a Study Director. This senior role requires 7+ years of clinical trial experience, including 3+ in global study leadership. You will manage cross-functional teams to ensure timely, high-quality delivery. The position offers competitive ben...

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 Sao Paulo. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive benefits including health insu...