iconplc - IT - Administration

Join a global pharmaceutical leader as a Site Investigational Product Specialist in Reading, UK. Utilize your extensive clinical trial and IP administration expertise (IV, SC, IM) in Oncology/Immunology. Ensure safe investigational product preparation and serve as the key liaison between sponsor ...

Join ICON plc as an In-House CRA in Ankara. Utilize your life sciences degree and clinical research skills to support site management, document compliance, and data oversight. Enjoy a comprehensive benefits package while contributing to global clinical development in a collaborative, fast-paced e...

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 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 as a Clinical Research Associate in São Paulo. 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 health insurance, competitive retirement plans, ...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing new therapies. This role requires a science degree, CRA experience, and 60% travel. We offer competitive health insurance, retirement ...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. The role requires a scientific degree, CRA experience, and 60% travel. We offer competitive health insurance and retirement plans.