This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Join ICON plc as a Contract Associate in Madrid, Spain. Leverage your 2+ years of contract management experience and law/business degree to draft, negotiate, and manage agreements in a world-leading clinical research organization. Enjoy home-based flexibility, comprehensive health insurance, reti...
Global Study Manager opportunity in Barcelona with ICON Strategic Solutions, embedded within a leading biopharmaceutical FSP team. You will oversee global clinical studies, manage vendors, and ensure ICH-GCP compliance. Requires 5+ years clinical research experience, 3+ in global project manageme...
Senior Clinical Research Associate sought by ICON Plc in Madrid to lead site monitoring and trial management. This role demands expertise in GCP, regulatory compliance, and data integrity, with 60% travel. Ideal candidates possess a scientific degree, strong organizational skills, and experience ...
Lead global clinical research projects as a Senior Project Manager at ICON plc in Barcelona. Utilize your pharmaceutical industry expertise to drive project execution and mentor teams. We offer competitive health insurance, retirement planning, and a supportive, innovative environment shaping the...
Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in Madrid or Barcelona. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer c...
Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role from Madrid. You will oversee clinical trial sites, ensuring protocol adherence, GCP compliance, and data integrity. This role requires extensive CRA experience, strong site management skills, and a willingness to tr...
Join ICON plc as a Clinical Research Associate II in a home-based role from Madrid. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We o...