iconplc

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 ICON plc as a Senior Clinical Research Associate in Sao Paulo. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive benefits including health insu...

Join ICON plc as a Senior Clinical Research Associate in Mexico City. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% domestic travel. Enjoy competitive benefits including ...

Join ICON plc as a Clinical Research Associate II in Mexico City. 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% domestic travel. We offer competiti...

Join ICON's AstraZeneca FSP program as a Global Clinical Trial Assistant. This home-based role requires 2+ years of global study support experience and ICH-GCP knowledge. You will manage the Trial Master File, coordinate study materials, and ensure regulatory compliance. We offer competitive heal...

Join ICON plc as a Senior Site Management Associate in Bucharest. Oversee clinical trial site operations, ensuring GCP compliance and high-quality data delivery. Requires extensive site management experience, fluency in Romanian, and strong problem-solving skills. We offer competitive health insu...

Lead global clinical trials from Mexico City as a Senior Clinical Trial Manager with ICON. Utilize your 7+ years of CTM experience, including expertise in North America and LATAM studies, to oversee budgets, drive enrollment, and ensure study integrity. Enjoy competitive benefits while shaping th...

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 as a Senior CRA or CRA in Blue Bell, USA. You will ensure protocol compliance and data integrity across clinical trial sites, requiring 1-3+ years of monitoring experience and ICH-GCP knowledge. This role involves ~60% travel and offers competitive health insurance, 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 Learning & Development Specialist in Blue Bell, US. You will support protocol-specific training planning within assigned therapeutic areas, ensuring GCP and SOP compliance. The role requires a Bachelor's degree and 2+ years of clinical trial experience. We offer competitive hea...

Join ICON plc as a Medical Research Associate in San Antonio. Support clinical trial design, execution, and data management, ensuring accuracy and quality. Requires a medical certification and strong organizational skills. Enjoy competitive benefits including health insurance and retirement plann...