iconplc - Remote work

Lead clinical research projects from home in Brazil for a global healthcare leader. Utilize your project management expertise to deliver high-quality results on time and within budget. Enjoy competitive benefits including health insurance and retirement planning. Join ICON plc to shape the future...

Join ICON plc as a Senior Clinical Trial Manager in a home-based role in Brazil. You will ensure successful study delivery, manage budgets, and drive enrollment for global trials. This sponsor-dedicated position requires extensive CRO/pharma experience and offers competitive health insurance and ...

Join ICON plc, a global clinical research leader, as a Research Operations Coordinator in the United States. Support project execution and clinical trial coordination within the pharmaceutical industry. Utilize your organizational skills and life sciences background in a dynamic team. Enjoy compe...

Seeking a Global Study Manager with 3+ years in clinical trial management, including phase I oncology. You will oversee global study execution, vendor management, and key document development. This remote US role (Eastern/Central time) offers competitive health insurance and retirement benefits a...

Lead strategic procurement for clinical trials as a Senior Manager at ICON. Utilize your IVRS expertise and healthcare sourcing background to drive cost efficiencies and supplier relationships. This US-based role offers competitive benefits, focusing on data-driven decisions and cross-functional ...

Join ICON plc as a Senior Clinical Research Associate in Copenhagen. 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 ins...

Join ICON plc, a global clinical research leader, as a remote CRA II based in France. Utilize your 24+ months of independent monitoring experience on Phase II/III commercial trials. You will take full ownership of investigator sites, ensuring data integrity and compliance. We offer competitive be...

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 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...