iconplc - China, 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 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 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...

Join ICON Plc in Shanghai as a Clinical Research Associate. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel. Enjoy health insurance, competitive retirement plans, and a global s...

Join ICON plc as a Clinical Research Associate II in Beijing. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This office-based role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirem...

Join ICON plc in Shanghai as a Clinical Research Associate. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning, an...

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 in Shanghai as a Clinical Research Associate II. You will monitor clinical trial sites, ensure protocol/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 in...

Join ICON plc as a Clinical Research Associate I in Beijing. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel readiness. We offer competitive health insurance, retirement plannin...

Join ICON plc as a Senior Clinical Research Associate in Beijing or Guangzhou. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive monitoring and site management expertise within a world-leading CRO. Enjoy competitive benefits...