iconplc - Research and Development, Remote work

Join ICON plc in Seoul as a Study Start Up Associate II and help shape the future of clinical development. You will lead clinical trial initiation, ensure regulatory compliance, and manage essential documents. This role requires 2+ years of study start-up experience and offers competitive health ...

Join ICON plc as a Pharmacometrician and shape the future of clinical development. Utilize your expertise in NONMEM/Monolix to drive regulatory strategy and analysis plans. This role requires a PhD and 3+ years of applied model-based drug development experience. Enjoy competitive benefits includi...

Join ICON plc in Warsaw as a Local Trial Manager. Oversee the planning and execution of clinical trials, ensuring compliance with timelines, budgets, and regulations. Leverage your scientific degree and therapeutic expertise to lead cross-functional teams and manage site relationships. This role ...

Join ICON plc as a Senior Clinical Research Associate in Athens, Greece. Oversee oncology clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires 12+ months of monitoring experience and offers extensive travel, competitive benefits, and a chance to sha...

Seeking a Senior Clinical Site Manager (CRA) for a part-time, home-based role in Melbourne or Sydney. This position requires extensive monitoring experience, GCP knowledge, and 50% travel. You will ensure protocol compliance and drive site performance for a leading pharmaceutical client. We offer...

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 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 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...