iconplc

Seeking a detail-oriented Clinical Research Coordinator for an office-based role in Gliwice/Bytom. You will support oncology studies, ensuring protocol and ICH-GCP compliance while managing site activities and data entry. This role requires fluency in English and Polish, along with proven oncolog...

Join ICON plc as a TMF Lead in Warsaw. Oversee Trial Master File management, ensuring regulatory compliance and integrity in clinical trials. Utilize your expertise in TMF processes within a world-leading clinical research organization. Enjoy competitive benefits including health insurance and re...

Join ICON plc as a Senior Clinical Research Associate in Johannesburg. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and participant safety. This role requires extensive CRA experience and a strong background in Respiratory studies, with 60% travel. We offer comp...

Join ICON plc as a Clinical Research Associate II in Frankfurt. You will design trials, analyze medical data, and ensure protocol compliance with 60% travel. Requires 2+ years CRA experience, ICH-GCP knowledge, and a scientific degree. We offer health insurance, competitive retirement plans, and ...

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 Dublin, Ireland. 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 p...

Join ICON plc, a global clinical research leader, as a Senior CRA in France. This remote role requires 3+ years of independent monitoring experience in Pharma/Biotech/CRO. You will manage full site ownership across key therapeutic areas like Oncology and Neurology. Enjoy a competitive package wit...