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Join ICON plc in Shanghai as a Clinical Research Associate (SSU). You will design trials, analyze complex medical data, and advance innovative therapies. We require 2+ years of CRA experience, ICH-GCP knowledge, and strong organizational skills. Enjoy competitive benefits including health insuran...

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

Join ICON plc as a Clinical Research Associate II in Guangzhou. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement pla...

Join ICON plc as a Clinical Research Associate II in Chengdu. You will monitor clinical trial sites, ensure protocol/GCP compliance, and manage data integrity. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel availability. We offer competitive health ins...

Seeking a Clinical Trial Manager for a home-based, client-dedicated role in Seoul. You will manage global trial operations, ensuring quality, timelines, and compliance. Requires 2+ years of CTM experience, therapeutic expertise, and fluent English. We offer competitive benefits including health i...

Join ICON in Seoul as a Clinical Research Associate II. Design and analyze trials, ensuring protocol compliance and data integrity with ICH-GCP expertise. This role requires 2+ years of CRA experience and offers competitive benefits, including health insurance and global support. Expect approxima...

Lead clinical trials from planning to completion in this home-based South Korea role. Oversee timelines, budgets, and compliance for non-oncology studies. Leverage your therapeutic expertise and monitoring skills in a world-leading CRO. Enjoy competitive benefits including health insurance and a ...

Join ICON as a Clinical Trial Liaison in Raleigh, USA. You will design and analyze oncology clinical trials, interpreting complex medical data. This role requires a life sciences degree and proven trial enrollment experience. We offer competitive health insurance, retirement plans, and a global s...

Join ICON plc, a global clinical research leader, as a Dietary Aid/Medical Research Representative in San Antonio. This PRN, day-shift role is vital for maintaining a clean, safe, and sanitized environment. Utilize your custodial skills and attention to detail in a supportive, innovative workplac...

Seeking a Manager for Data Monitoring Committee and Endpoint Adjudication projects. This role involves overseeing clinical trial projects, managing a team, and ensuring regulatory compliance with GCP/ICH guidelines. It offers a competitive benefits package and requires approximately 30% travel.

Join ICON plc, a global clinical research leader, as a Senior Clinical Research Associate in Oncology. This remote East Coast role requires 5+ years of monitoring experience, including site feasibility and start-up, with a focus on ICH-GCP. We offer competitive health insurance, retirement planni...

Lead clinical data science programs at ICON in Blue Bell. Oversee complex data-driven projects from collection to insight implementation. Requires a strong background in data science, program management, and cross-functional leadership. We offer competitive health insurance, retirement plans, and...