iconplc - IT - Administration, On-site work

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...

Join ICON plc's clinical research team in Houston as a Medical Research Associate. Support the design and execution of trials, ensuring data accuracy and quality. Requires a medical certification and strong organizational skills. Enjoy competitive benefits including health insurance and retiremen...

Join ICON plc as a Clinical Trial Administrator in Mexico City. Support the design and analysis of clinical trials, ensuring protocol compliance and managing essential documentation. This role requires a scientific degree, knowledge of trial processes, and strong organizational skills. We offer c...

Join ICON plc as a Pharmacovigilance Associate in Chennai. Process Clinical Trial cases using your LSMV database skills and 2+ years of PV experience. Ensure patient safety by analyzing adverse events and maintaining regulatory compliance. Enjoy competitive benefits including health insurance and...

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate in Chennai. Utilize your scientific degree and organizational skills to coordinate trials and manage essential documentation. This role offers competitive benefits and a chance to contribute to innovative healthcare a...

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 Seoul as a Clinical Trial Associate. You will coordinate trials, ensure regulatory compliance, and manage essential documentation. This role requires a science degree, knowledge of trial processes, and excellent organizational skills. We offer competitive health insurance, retire...

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...