iconplc

Join ICON plc as a Senior Clinical Research Associate (CRA) in Denmark, working remotely. 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 compet...

Join ICON plc as a Clinical Research Associate II in Seoul. You will design trials, analyze complex medical data, and advance innovative therapies. Requires 2+ years of onsite monitoring experience and ICH-GCP knowledge. We offer competitive health insurance, retirement planning, and a supportive...

Join ICON plc as a Clinical Research Associate II in Bangkok. You will design trials, analyze medical data, and ensure protocol compliance and patient safety. Requires 2+ years of onsite monitoring experience and ICH-GCP knowledge. We offer competitive health insurance, retirement planning, and a...

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

Join ICON plc as a Senior Clinical Research Associate in Rome. 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 benefits including he...

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

Join ICON Plc in Shanghai as a Clinical Research Associate. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a global s...

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

Join ICON Plc as a Senior Clinical Research Associate in Frankfurt. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive monitoring and site management expertise in a role requiring ~60% travel. Enjoy competitive benefits inclu...

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

Join ICON Plc as a Senior Clinical Research Associate in Milan. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy health insurance, competitive retirement plans, and glo...

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