iconplc

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

Join ICON plc in São Paulo as a Senior Clinical Research Associate. 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 health insurance, retirement p...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, site management expertise, and domestic travel. We offer competitive benefits inc...

Join ICON plc as a Senior Clinical Research Associate and help shape the future of clinical development. You will monitor sites, ensure protocol/GCP compliance, and contribute to innovative treatments. This role requires 9+ months of monitoring experience and 60% travel across the US. We offer co...

Join ICON plc as a Clinical Site Associate in Tel Aviv. Support site management for clinical trials, ensuring efficiency and compliance. A life sciences degree and strong organizational skills are key. Enjoy a hybrid role with competitive health insurance and retirement benefits.

Join ICON plc as a Senior Clinical Research Associate (CRA) in a remote role based in Blue Bell, US. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This position requires extensive CRA experience, strong site management skills, and 60% travel. ...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in Germany. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and a willingness to travel ...

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

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

Join ICON plc's dynamic team in Seoul as a Regulatory Affairs Specialist. You will design clinical trials, interpret medical data, and prepare key submissions (CT/IND, MAA/NA). This role requires 2-3 years of pharmaceutical regulatory experience. We offer competitive health insurance, retirement ...

Join ICON plc as an Echocardiography Technician in Salt Lake City. Perform key cardiac diagnostic procedures like ECGs and stress tests within clinical research. This PRN, day-shift role requires relevant certification and hospital experience. Contribute to patient safety and excellence in cardio...

Join ICON plc, a global clinical research leader, as a Clinical Research Nurse I in San Antonio, TX. Utilize your Texas RN license and 1-2 years' nursing experience to coordinate trials, ensure protocol adherence, and provide patient care. This PRN, day-shift role offers competitive benefits with...