iconplc - Research and Development

Join ICON plc as a Clinical Site Associate in Kuala Lumpur. Support global clinical trials, managing site communications, TMF/ISF documents, and ensuring GCP compliance. Requires a life sciences degree and strong organizational skills. Enjoy health insurance, competitive retirement plans, and a s...

Join ICON plc in Shanghai as a Clinical Research Associate II. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive heal...

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Romania. This remote, client-dedicated role involves monitoring Phase I-IV trials across therapeutic areas, requiring 3.5+ years of independent monitoring experience and 60% travel. We offer competitive b...

Join ICON plc as a Clinical Research Associate II in Sao Paulo. 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 health i...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate. Utilize your 2-3 years of monitoring experience across therapeutic areas to drive site start-up in Texas. You will ensure GCP compliance, build key site relationships, and support patient recruitment. This role of...

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 as a Senior Clinical Research Associate (CRA) in Mechelen. Independently manage all trial site activities from start-up to close-out, ensuring protocol and SOP compliance. Enjoy a competitive package with health insurance and support programs, while making a real impact on global pa...

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,...

Join our Portland team as a Senior Research Associate to develop and validate cutting-edge molecular assays for clinical trials. You will design studies, analyze data, and collaborate cross-functionally, leveraging 3+ years of lab experience and PCR expertise. We offer competitive benefits includ...

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...

Join our winning lab team at ICON plc, a top-rated employer. We seek a Scientist II in Whitesboro, NY to develop and perform GLP/GCP assays for clinical trials. The role requires a Bachelor's in Biology/Chemistry and experience with binding assays. We offer a competitive salary, bonus, and compre...