Remote Jobs at ICON plc
Find your next remote opportunity · 126 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 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.
Clinical Research Associate 1
In Vitro Diagnostics CRA conducting clinical research studies for ICON, a global healthcare intelligence and clinical research organisation. Monitoring trials, validating product claims, and supporting regulatory submissions.
Study Delivery Specialist
Study Delivery Specialist supporting clinical trial site monitoring for ICON, a global clinical research organization. Ensuring protocol compliance, site documentation, performance tracking, and monitoring reports.
Clinical Project Manager
Clinical Project Manager leading US clinical projects for ICON, a global clinical research organization. Coordinating timelines, budgets, risks, stakeholders, and cross-functional teams.
Clinical Trial Liaison
Clinical Trial Liaison supporting ICON, a global clinical research organisation, through investigator management and enrollment strategy. Advancing clinical trials, site performance, and innovative treatments across eligible US states.
Site Selection Lead
Site Selection Lead directing clinical trial site strategy and feasibility for ICON, a global healthcare intelligence and clinical research organization. Delivering compliant, high-performing site selections and activation milestones.
Clinical Research Associate
Clinical Research Associate monitoring early-development clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Conducting site visits, ensuring ICH-GCP compliance, and maintaining data integrity and patient safety.
Clinical Associate
Clinical Associate supporting clinical trials at ICON, a global healthcare intelligence and clinical research organization. Coordinating study sites, patient recruitment, data collection, monitoring, documentation, and close-out activities.
Contract Analyst I
Contract Analyst managing invoicing and contract activities within clinical research for ICON. Collaborating with internal teams and ensuring compliance with budgeting and clinical agreements.
Contract Analyst I
Contract Analyst at ICON preparing invoicing and managing clinical trial agreements. Collaborating with various teams to enhance contract management processes and resolve issues.