iconplc - Research and Development

Join ICON plc as a Senior Clinical Research Associate in Milan. 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 insuranc...

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. 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...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate. Utilize your Study Coordinator experience to support trial operations, ensure site compliance, and manage documentation. This remote US role offers competitive benefits in a dynamic, mission-driven environment.

Join ICON plc as a Senior Clinical Research Associate in Oslo. Oversee clinical trials, ensure ICH-GCP compliance, and analyze data. Requires fluency in Norwegian and English, plus 60% travel. Enjoy health insurance, competitive retirement plans, and a global support program.

Join ICON plc in Hong Kong as a Clinical Research Associate II. You will monitor clinical trial sites, ensure ICH-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 insura...

Seeking an experienced Senior Clinical Research Associate (CRA) for oncology trials in the Midwest. You will monitor sites, ensure GCP compliance, and manage stakeholder relationships. This role offers competitive benefits including health insurance and requires extensive CRA experience with onco...

Join ICON plc as a Clinical Research Associate II in a remote role based in Colombia. 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 insuran...

Join ICON Plc as a Clinical Research Associate in Utrecht. Oversee clinical trials, ensuring protocol adherence, GCP, and data integrity. This role requires a life sciences degree, CRA experience, and 60% travel. We offer health insurance, competitive retirement plans, and global support.

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,...