iconplc - China, IT - Administration

Join ICON plc as a Clinical Research Associate II in Hangzhou. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive health in...

Join ICON plc in Beijing as a Clinical Research Associate II. 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 planning,...

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. This role requires extensive CRA experience, strong site management skills, and a willingness to travel 60%. We offer ...

Join ICON plc as a Senior Clinical Research Associate in Beijing. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement...

Join ICON plc as a Clinical Research Associate II in Wuhan, China. 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 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 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 in Nanjing as a Clinical Research Associate II. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity in global clinical trials. This role offers significant travel, competitive benefits, and a chance to shape the future of clinical...

Join ICON plc as a Clinical Research Associate II in Chengdu. 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 ins...