iconplc - Remote work

Launch your pharmacovigilance career at ICON in Warsaw. Utilize your life sciences degree to process safety data, ensuring compliance and patient safety. This graduate role offers extensive training, collaboration with global teams, and a comprehensive benefits package. Strong English and Polish ...

Join ICON plc as a Global Delivery Manager and shape the future of clinical development. You will manage end-to-end clinical study delivery, ensuring quality, timelines, and budget. The role requires 5+ years in clinical research, strong ICH-GCP knowledge, and excellent project leadership. We off...

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 ...