iconplc - Research and Development

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% ...

Join ICON plc as a Clinical Research Associate I in Beijing. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel readiness. We offer competitive health insurance, retirement plannin...

Join ICON plc, a global clinical research leader, as a Clinical Study Coordinator in Salt Lake City. You will design trials, analyze medical data, and advance innovative therapies. The role requires a scientific degree, GCP knowledge, and strong organizational skills. We offer competitive benefit...

Join ICON plc as a Clinical Research Associate I/II in Ankara. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor trials and ensure data integrity. This role requires fluency in English and Turkish. We offer competitive benefits including health insurance and a global suppor...

Join our team in Mexico City as a Regulatory Technician. You will manage clinical trial submissions using the CTIS system, ensuring compliance and quality. Ideal candidates have advanced English and 1-2 years in clinical research. We offer competitive health insurance and retirement plans.

Join ICON plc, a global clinical research leader, as a Senior CRA or CRA II in Blue Bell. Utilize your monitoring experience and ICH-GCP knowledge to ensure trial integrity and patient safety. This role offers significant travel, competitive benefits, and a chance to shape the future of healthcare.

Join ICON plc as a Clinical Research Associate II in São Paulo. You will design trials, analyze complex medical data, and ensure protocol compliance with ICH-GCP. This role requires a scientific degree, on-site monitoring experience, and 60% travel. We offer competitive health insurance and retir...

Join ICON plc as a Senior Clinical Research Associate in Taipei. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...

Join ICON plc in Budapest as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, re...

Join ICON plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive monitoring and site management expertise within a world-leading CRO. Enjoy competitive benefits...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Reading, UK. Support trial operations by ensuring site compliance, documentation accuracy, and audit readiness. This role requires a life sciences degree, strong organizational skills, and offers competitive benefit...

Join ICON plc as a Clinical Site Associate in Paris. Support clinical trial operations, ensure site compliance, and manage documentation in French and English. This office-based role offers a clear path to a travelling CRA position within a year, with comprehensive benefits.