iconplc - China, Shanghai, IT - Administration

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 ...

Lead clinical trial operations in Shanghai as a Manager at ICON plc. Oversee global study execution, ensuring regulatory compliance and on-time delivery. Requires a Bachelor's in science/healthcare, extensive clinical ops experience, and strong leadership skills. Enjoy benefits like health insura...

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 Plc as a Clinical Research Associate II in Shanghai, China. Oversee global clinical trials, ensure ICH-GCP compliance, and manage study documentation. Requires a science degree, strong communication skills, and 60% travel. Enjoy competitive benefits including health insurance, retiremen...

Join ICON as a Clinical Research Associate II (CRA II) in Shanghai, China. Leverage 2+ years of experience and ICH-GCP expertise to design, monitor, and analyze clinical trials. Ensure protocol compliance and data integrity while traveling up to 60%. Enjoy competitive benefits including health in...

Join ICON plc as a Contract Analyst II in Beijing or Shanghai. Leverage your 2+ years of contract administration experience and legal expertise to review, negotiate, and manage clinical trial agreements. Collaborate with cross-functional teams to ensure regulatory compliance and mitigate risks. E...

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...