iconplc

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Singapore. You will design trials, analyze medical data, and ensure protocol compliance with 60% travel. Requires 2+ years CRA experience, ICH-GCP knowledge, and a life science degree. We offer competitive he...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in France. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, Phase I Oncology expertise, and 60% travel. We offer ...

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Shenyang. You will design and analyze trials, ensure protocol compliance, and advance innovative therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitiv...

Join ICON plc as a Clinical Research Associate II in Kuala Lumpur. 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. We offer competitive health insurance, ...

Lead clinical trial monitoring and site management in Prague as a Senior CRA for ICON Plc. Utilize your extensive CRA experience to ensure protocol adherence, GCP compliance, and data integrity across multiple sites. This role offers competitive benefits and involves approximately 60% travel. Dri...

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 ...