iconplc - Research and Development

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...

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...

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...