iconplc

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...

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.

Seeking a Senior Data Scientist specializing in Data Management for a remote US role. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient data linkage. This position offers competitive benefits and the chance to drive healthcare innovation with ICON p...

Lead clinical data science programs at ICON, managing end-to-end project execution within scope and budget. Utilize your expertise in data science, statistics, and cross-functional leadership to drive clinical outcomes. This US-based role offers competitive health insurance, retirement planning, ...

Lead early-phase oncology trials as a Clinical Trial Manager at ICON in Raleigh or Blue Bell. Utilize your 5+ years of experience, including oncology and multinational trial management, to drive study success. This role offers competitive benefits and focuses on vendor oversight and regulatory co...

Join ICON plc, a global clinical research leader, as a Senior Contract Analyst in Blue Bell, US. You will manage and negotiate clinical trial contracts, ensuring compliance and mitigating risks. The role requires a business/legal degree, industry experience, and strong analytical skills. We offer...