iconplc

Join ICON plc in Milan as a Clinical Research Associate II. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning, a...

Join ICON plc as a Senior CRA in Guangzhou. You will conduct site monitoring, ensure protocol/GCP compliance, and contribute to advancing clinical trials. This role requires 2+ years CRA experience, deep trial knowledge, and 60% travel. We offer competitive health insurance, retirement plans, and...

Join ICON plc as a Clinical Research Associate II in Prague. 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 insu...

Join ICON plc as a Senior Clinical Research Associate in Warsaw. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...

Join ICON plc in Shanghai as a Clinical Research Associate II. 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 in...

Join ICON plc as a Senior Clinical Research Associate in Paris. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, re...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate. This role focuses on study start-up support and vendor management within the US. We seek organized professionals with CRO/pharma experience and strong communication skills. Enjoy competitive benefits including health...

Lead regional clinical trial operations for a global CRO. This Boston or Philadelphia-based role requires 5-7 years' experience, including 3+ years in trial execution and direct team management. Oncology/hematology expertise is preferred. We offer a competitive salary, comprehensive benefits, and...

Join our dynamic team in San Antonio as a Medical Research Associate. Support clinical trial design, execution, and data management, ensuring accuracy and compliance. Ideal candidates have medical certification, strong organizational skills, and research software proficiency. We offer competitive...

Seeking an Associate Director of Regional Clinical Operations to oversee clinical trials in the Southern US (Atlanta, Houston, Tampa, Dallas). This role requires 5-7 years in clinical operations, including 3+ years in trial execution and direct team management. Ideal candidates have global trial ...

Join ICON plc as a Site Activation and Maintenance Associate I in Raleigh or Blue Bell. You will manage 25-30 sites, handling regulatory documents, IRB communication, and compliance. This role requires a Bachelor's degree and clinical research experience. We offer competitive health insurance, re...

Join ICON plc in Mexico City as a Senior Clinical Data Science Programmer. Utilize your advanced SAS, R, or Python skills to develop programming solutions for clinical trial data analysis and reporting. You will ensure data accuracy and efficiency in a collaborative, cross-functional environment....