iconplc

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...

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...