Remote Jobs at ICON plc
Find your next remote opportunity · 135 Open Positions
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries.
We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Clinical Research Associate
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study data.
Clinical Data Manager
Clinical Data Manager leading clinical trial data management and data quality for ICON, a global clinical research organisation. Owning study data from start-up through database lock and close-out.
Study Start Up Associate II
Study start-up specialist launching clinical trials for ICON, a global healthcare intelligence and clinical research organization. Managing regulatory submissions, approvals, and site activation.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and research organization. Ensuring protocol compliance, data integrity, site performance, and regulatory standards.
Site Management Associate I, French Speaker, Payment Focused
Site Management Associate supporting clinical trial monitoring and compliance for ICON, a global healthcare intelligence and clinical research organisation. French- and English-speaking role focused on payment-related site management.
Study Start Up Associate I
Study Start-Up Associate facilitating regulatory submissions and site activation for ICON, a global healthcare intelligence and clinical research organisation. Supporting clinical trials that bring new treatments to patients faster.
Senior Medical Coding Specialist
Senior Medical Coding Specialist leading clinical-trial medical coding at ICON, a global healthcare intelligence and research organization. Ensuring accurate, compliant data using MedDRA and WHO Drug Dictionary.
Senior Clinical Data Coordinator
Senior Clinical Data Coordinator managing clinical trial data for ICON, a global clinical research organisation. Creating data management plans, resolving discrepancies, and mentoring junior coordinators.
Senior Clinical Data Coordinator
Senior Clinical Data Coordinator managing clinical trial data at ICON, a global healthcare intelligence and clinical research organization. Supporting data quality, regulatory compliance, and faster delivery of new medicines and treatments.
Clinical Research Lead
Site Engagement Liaison building clinical trial site relationships for ICON, a global healthcare intelligence and clinical research organisation. Supporting study compliance, engagement strategies, and site performance.
Principal Clinical Data Standards Consultant
Principal consultant developing CDISC-compliant data standards for ICON’s global clinical research organization. Advising sponsors, governing standards, and delivering training across clinical trials.
Graduate Pharmacovigilance Associate
Graduate Pharmacovigilance Associate supporting drug safety at ICON, a global clinical research organisation. Processing adverse events, preparing safety reports, and maintaining pharmacovigilance documentation.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing oncology Phase I trials for ICON, a global clinical research organisation. Managing investigative sites, monitoring data integrity, and ensuring patient safety and inspection readiness.
Clinical Research Associate 2
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study delivery.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring oncology trials for ICON, a global clinical research organisation. Conducting site visits, ensuring compliance, and overseeing patient safety, data quality, and site performance.
Clinical Research Associate – Oncology
Clinical Research Associate monitoring oncology and hematology trials for ICON, a global clinical research organization. Conducting site visits, ensuring compliance, and supporting patient safety and data quality.
Project Manager – Hematology/Oncology
Project Manager coordinating oncology/hematology clinical-trial projects for ICON, a global healthcare intelligence and clinical research organization. Managing timelines, budgets, risks, stakeholders, and cross-functional teams for pharmaceutical clients.
Senior Project Manager
Senior Project Manager leading clinical outcome assessment localization and eCOA programs at ICON, a global clinical research organization. Managing multilingual content, migrations, licensing, quality, and automation across pharmaceutical studies.
Senior Clinical Associate
Senior Clinical Associate overseeing clinical trials for ICON, a global clinical research organisation. Coordinating sites, ensuring regulatory compliance, maintaining data integrity, and mitigating study risks.
Study Start-Up Lead
Study Start-Up Lead coordinating global clinical trial activation for ICON, a clinical research organisation. Managing documents, submissions, vendors, budgets, and site readiness to accelerate patient access to medicines.