iconplc

Lead complex clinical trial programs as a Trial Delivery Lead at ICON in Blue Bell. Utilize your extensive program management expertise to deliver large-scale projects on time and within budget. This role offers competitive benefits and requires strong leadership to guide cross-functional teams.

Join ICON plc as a Clinical Research Associate II in Buenos Aires. 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 plan...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in China. You will monitor sites, ensure protocol/GCP compliance, and advance innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competiti...

Join ICON plc as a Clinical Research Associate (CRA) in Mechelen, Belgium. You will monitor clinical trial sites, ensuring protocol and GCP compliance. The role requires a life sciences degree, Dutch and English fluency, and proven monitoring experience. We offer competitive benefits including he...

Join ICON plc as a Clinical Research Associate II in Montreal. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing new therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance,...

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

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...