iconplc - Remote work

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 as a Senior Statistical Programmer II in Montreal (remote). Utilize your advanced SAS and R-Shiny skills to analyze clinical trial data, ensuring statistical integrity. This role offers competitive benefits and a chance to shape the future of clinical development within a global lea...

Join ICON plc as a fully remote, client-dedicated Pharmacometrician. Utilize your Ph.D. and 3+ years of experience in model-based drug development, with expertise in NONMEM and Monolix. You will drive pharmacometric strategy for regulatory submissions and collaborate with multidisciplinary teams,...

Lead regulatory submissions and strategy as a home-based Manager in Seoul. Utilize 6+ years of pharmaceutical regulatory experience to guide drug development from CTA to post-approval. Enjoy competitive benefits including health insurance and global support, driving excellence at a world-leading ...

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...