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 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 II in a home-based role across Australia. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity in clinical trials. This pivotal role offers extensive travel, competitive benefits, and the chance to ...

Join ICON plc, a global healthcare intelligence leader, as a Contract Analyst II in Dalian. Utilize your finance or accounting degree to manage invoicing, client relationships, and account reconciliation for a portfolio of clinical research accounts. This role offers competitive benefits, includi...

Join ICON plc in Reading as a Senior Clinical Supplies Project Manager. Lead clinical supply projects, ensuring timely delivery for global trials. Utilize your 5+ years of supply chain experience to optimize processes and ensure regulatory compliance. Enjoy competitive benefits while shaping the ...

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 ...