iconplc - IT - Administration, On-site work

Join ICON plc, a global clinical research leader, as a Clinical Research Coordinator in San Antonio, TX. You will coordinate early-phase studies, ensuring protocol and ICH-GCP compliance while managing participant care and data. This role requires a scientific degree, research experience, and str...

Seeking a detail-oriented Clinical Research Coordinator for an office-based role in Gliwice/Bytom. You will support oncology studies, ensuring protocol and ICH-GCP compliance while managing site activities and data entry. This role requires fluency in English and Polish, along with proven oncolog...

Join ICON plc in Mexico City as a Clinical Trial Associate. You will coordinate clinical trials, manage documentation, and ensure protocol compliance. We seek a detail-oriented graduate with clinical research knowledge and strong organizational skills. Enjoy competitive benefits including health ...

Join ICON plc as a Clinical Site Associate in Paris. Support clinical trial operations, ensure site compliance, and prepare for audits while building skills towards a CRA role. Requires a life sciences degree, fluency in French/English, and offers comprehensive benefits. This office-based positio...

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...