iconplc - Research and Development

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...

Join ICON plc as a Clinical Site Associate in Milan, Italy. Support clinical trial operations by ensuring site compliance, documentation accuracy, and audit readiness. Requires a life sciences degree, clinical research experience, and fluency in Italian and English. Enjoy competitive benefits inc...

Join ICON plc in Mexico City as a Study Start-Up Associate II. Utilize your 2-4 years of clinical start-up experience and regulatory knowledge to support site activation and submissions. This role offers competitive benefits, including health insurance and retirement planning, in a global leader ...

Lead bioanalytical laboratory operations at ICON in Whitesboro, NY. Oversee a team, manage workflows, and ensure GLP compliance to deliver high-quality data for clinical trials. Requires a relevant degree, lab management experience, and strong leadership skills. We offer competitive health insura...

Join ICON plc as a Scientist I in Whitesboro, NY. You will develop and perform assays for clinical trials, ensuring compliance with GLP/GCP standards. The role requires a Bachelor's in Biology or related field and experience with binding assays. We offer a competitive salary, annual bonus, and co...

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 Clinical Site Associate in Bangkok. You will ensure site compliance, manage documentation, and support audit readiness for clinical trials. This role requires a life sciences degree, strong organizational skills, and fluency in English. Enjoy...

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...