iconplc - Remote work

ICON plc seeks a Clinical Supplies Project Manager to join its world-leading clinical research team in Warsaw or Gdansk, Poland. You will manage global supply planning, forecasting, and IRT system setup for clinical trials. Ideal candidates bring 4+ years of clinical supply experience, strong pro...

Lead clinical trials as Director, Clinical Operations at ICON in Sofia, Warsaw, Belfast, Poland, or Ireland. Drive performance, ensure GCP compliance, and manage cross-functional teams to advance innovative therapies. Requires a life sciences degree and extensive CRO/pharma experience. Enjoy comp...

Senior Clinical Research Associate (CRA) with oncology experience needed in Paris, France. Join ICON, a world-leading clinical research organization, to manage sites independently while ensuring ICH GCP and French regulatory compliance. Requires 4+ years of monitoring experience, fluency in Frenc...

Seeking a Senior Clinical Site Manager (SCRA) for a rare, home-based, part-time FSP role (0.6 FTE) in Adelaide or Melbourne. Leverage your CRA II/Senior CRA expertise to build strong site relationships, drive patient recruitment, and ensure audit-ready studies for a leading biopharma. Enjoy flexi...

Join ICON as a Senior CRA in Montreal, Canada, and lead Oncology study monitoring in a sponsor-dedicated role. Leverage your ICH-GCP expertise and medical/science degree to ensure patient safety and data quality. Enjoy 60% travel, competitive benefits including health insurance and retirement pla...

Join ICON as a UK home-based Clinical Research Associate 1, specializing in In Vitro Diagnostics. This unique role offers a transition from lab-based work into clinical trial operations on a blue-chip diagnostics project. You will coordinate study initiation, monitoring, and completion while ensu...

Join ICON as a home-based Clinical Research Associate in the UK. Leverage your ICH-GCP expertise and monitoring experience to oversee clinical trials, ensuring patient safety and data quality. This role requires a science degree, UK driving licence, and 40% travel to hospital sites. Enjoy flexibl...

Senior CRA, home-based in Poland. Join ICON, a world-leading clinical research organization, to oversee trial activities ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from flexible work, he...

ICON plc seeks a Clinical Research Associate II (XTA) in Chicago. Leverage 2+ years of on-site monitoring experience across multiple therapeutic areas. Ensure site compliance with ICH-GCP and manage visits using CTMS/eTMF. Enjoy competitive benefits, annual leave, and up to 50% travel across the ...

Join ICON plc as a Clinical Research Associate in Montreal, Canada. Monitor multi-therapeutic area studies in a sponsor-dedicated program, focusing on Oncology. Leverage your ICH-GCP expertise and medical knowledge to ensure patient safety and data quality. Enjoy competitive benefits, including h...

Join ICON plc as a Senior Clinical Research Associate in Seoul. 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 health insurance, retirement plann...

Regulatory Affairs Associate needed in Seoul, South Korea. Leverage 3+ years of clinical regulatory experience, including IND submissions and CMC, to drive study start-up activities. Ensure compliance, manage ethics submissions, and safeguard patient welfare through informed consent review. Benef...