iconplc - China, On-site work

Join ICON as a CRA II in Shanghai and drive clinical trial excellence. Leverage 2+ years of experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy competitive benefits including health insurance, retirement planning, and global ...

Join ICON as a Clinical Research Associate in Beijing, China. Leverage 2+ years of CRA experience and a scientific degree to design, monitor, and analyze clinical trials. Ensure ICH-GCP compliance, data integrity, and patient safety through site visits and collaboration. Advance innovative therap...

ICON seeks a Clinical Research Associate I in Shanghai to design and monitor clinical trials, ensuring ICH-GCP compliance and data integrity. Ideal candidates hold a Bachelor's in science/healthcare with 1+ year CRA experience. This role involves site visits, protocol oversight, and collaboration...

Join ICON as a Clinical Research Associate (CRA II) in Beijing, China. Leverage 2+ years of experience and ICH-GCP expertise to design, monitor, and analyze clinical trials. Ensure data integrity and patient safety while collaborating with investigators. Enjoy competitive benefits including healt...

ICON seeks a Clinical Research Associate II in Wuhan, China, to design and analyze clinical trials. You will conduct site monitoring, ensure ICH-GCP compliance, and safeguard data integrity. Requires a Bachelor’s degree and 2+ years of CRA experience. Enjoy competitive benefits, health insurance,...

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, 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, 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 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...