iconplc - United States, Remote work

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health i...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, expertise in GCP, and 60% travel. We offer competitive hea...

Join ICON plc as a Senior Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, strong monitoring skills, and 60% travel. We offer competi...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Clinical Research Associate in Ophthalmology, based in the United States. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We of...

Join ICON plc as a Clinical Research Associate in the United States. 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% travel. We offer competitive hea...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate. Oversee trial sites, ensure GCP compliance, and manage data integrity across multiple projects. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competiti...

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 (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% ...

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...