iconplc - IT - Administration, Hybrid work

Join ICON plc as a Senior Validation Engineer in Blue Bell, PA or Raleigh, NC. This office-based role with remote flexibility requires 10+ years of CSV/GxP experience. You will lead validation for complex global projects, ensuring compliance with FDA and EMA regulations. We offer competitive heal...

Lead clinical trials from planning to execution in Taipei, Taiwan. This pivotal role requires extensive operations management experience and strong leadership skills to ensure regulatory compliance and trial efficiency. You will mentor teams and drive innovation in a world-leading clinical resear...

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...