iconplc - Hybrid work

Join ICON plc as a Clinical Research Associate II in Puerto Rico. 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...

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 Clinical Site Associate in Milan, Italy. Support clinical trial operations by ensuring site compliance, documentation accuracy, and audit readiness. Requires a life sciences degree, clinical research experience, and fluency in Italian and English. Enjoy competitive benefits inc...

Join ICON plc in Mexico City as a Study Start-Up Associate II. Utilize your 2-4 years of clinical start-up experience and regulatory knowledge to support site activation and submissions. This role offers competitive benefits, including health insurance and retirement planning, in a global leader ...

Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Bangkok. You will ensure site compliance, manage documentation, and support audit readiness for clinical trials. This role requires a life sciences degree, strong organizational skills, and fluency in English. Enjoy...

Join ICON plc as a Senior Clinical Research Associate (CRA) in Mechelen. Independently manage all trial site activities from start-up to close-out, ensuring protocol and SOP compliance. Enjoy a competitive package with health insurance and support programs, while making a real impact on global pa...

Seeking a Senior Data Scientist specializing in Data Management for an office-based role in Blue Bell, PA or Raleigh, NC. You will design advanced models and algorithms, leveraging expertise in RCM processes and patient linkage methodologies. This role offers competitive benefits and the chance t...

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 plc, a global clinical research leader, as an Accounts Receivable Associate in Chennai or Trivandrum. You will manage the full Contract-to-Cash billing cycle, ensuring accurate invoicing and compliance. The role requires 2-3 years' AR experience, outstanding Excel skills, and collaborat...

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 ...