iconplc - IT - Administration, Hybrid work

Join ICON plc, a global clinical research leader, as a Clinical Research Associate II in Santiago, Chile. You will design trials, analyze complex medical data, and advance innovative therapies. The role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...

Join ICON plc, a global leader in clinical research, as a Clinical Site Associate in Warsaw. This hybrid role is key to ensuring site compliance and documentation accuracy for clinical trials. We seek a detail-oriented professional with a life sciences degree and strong organizational skills. Enj...

Join ICON plc as a Senior Clinical Data Coordinator in Mexico City. Utilize your 5-7 years of experience with RAVE or Veeva to ensure data quality and regulatory compliance. You will develop data management plans, mentor junior staff, and collaborate with cross-functional teams. We offer competit...

Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...

Join ICON in San Antonio as a CMC Project Manager I. You will lead CMC projects for early-phase drug development, ensuring GMP compliance and coordinating cross-functional teams. This role requires 1+ years of project management experience in a pharmaceutical setting. We offer competitive health ...

Join ICON plc, a global clinical research leader, as a Project Manager I EDS. This hybrid role in Whitesboro, NY requires 3+ years of lab or project management experience. You will manage bioanalytical project timelines, budgets, and client coordination. We offer competitive health insurance, ret...

Join ICON plc as an In-House CRA in Ankara. Utilize your life sciences degree and clinical research skills to support site management, document compliance, and data oversight. Enjoy a comprehensive benefits package while contributing to global clinical development in a collaborative, fast-paced e...

Join ICON plc as a Clinical Site Associate (In-House CRA) in Hong Kong. Support clinical trial operations, ensuring site compliance and documentation accuracy in this hybrid office role. Utilize your life sciences background and organizational skills within a world-leading CRO. Enjoy competitive ...

Join our Pharmacovigilance team in Warsaw or Sofia as an Administrative Assistant. Play a vital role in global projects, ensuring compliance and patient safety through meticulous administrative support. A life sciences background is beneficial. We offer competitive benefits including health insur...