iconplc - China, IT - Administration

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Shanghai. Utilize your life sciences degree and clinical research experience to support trial design, implementation, and monitoring. You will ensure protocol adherence and data integrity while collaborating with c...

Join ICON plc in Guangzhou 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 i...

Join ICON in Shanghai as a Site Specialist II, a key role in clinical trial execution. You will conduct site visits, ensure protocol/GCP compliance, and manage data integrity. Requires a Bachelor's degree, 3+ years of SSU experience, and strong organizational skills. We offer competitive benefits...

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

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...