iconplc - Research and Development

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...

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.