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 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, a global clinical research leader, as a Site Management Associate I in Kuala Lumpur. Support site monitoring and ensure protocol/GCP compliance in a dynamic team environment. A relevant degree and strong organizational skills are key. Enjoy competitive health insurance, retirement ...
Join ICON plc, a global clinical research leader, as a Clinical Trial Assistant in Manila. Utilize your scientific background to coordinate trials, manage documentation, and ensure regulatory compliance. Enjoy competitive benefits while contributing to innovative healthcare advancements in a dyna...
Lead regional pharmacovigilance activities for a global CRO. Oversee drug safety projects, ensure GVP compliance, and enhance safety processes. Requires 7-12 years' industry experience, including 5+ in PV. Offers competitive health insurance and retirement planning.
Location
Salary
Not provided
iconplc
Expiration Date
Until further notice
Manager, Clinical Operations
Lead clinical trial operations in Warsaw, ensuring efficiency and regulatory compliance. This pivotal role requires extensive experience in managing clinical operations and strong leadership skills. You will drive strategic planning, mentor teams, and contribute to innovative therapies. We offer ...
Join ICON plc, a global healthcare intelligence leader, as a Global Clinical Delivery Manager in Sofia. Utilize your 5+ years of clinical research experience and project management skills to coordinate international trials from setup to archival. You will ensure study delivery to time, cost, and ...
Join ICON plc, a global clinical research leader, as a CRA II/Senior CRA. Support high-impact trials for a large pharmaceutical company from Paris or Lyon. Requires 2+ years of monitoring experience, ICH-GCP knowledge, and fluency in French/English. Enjoy competitive benefits and shape the future...