Remote Jobs at ICON plc
Find your next remote opportunity · 187 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.
Site Contracts Negotiator
Site Contracts Negotiator negotiating clinical trial agreements and site budgets in Poland. Supporting ICON's global healthcare intelligence and clinical research operations.
Feasibility Analytics Manager – Advanced
Feasibility Analytics Manager delivering clinical trial analytics, feasibility insights, and enrollment modelling for ICON’s sponsor-dedicated FSP services. Driving data, technology, and operational improvements across global development.
Graduate Pharmacovigilance Associate
Graduate Pharmacovigilance Associate supporting adverse-event processing and safety reporting for ICON’s pharmaceutical sponsors. Remote, home-based role in Mexico City.
Senior Clinical Scientist
Senior Clinical Scientist leading HIV clinical trials for ICON Strategic Solutions’ sponsor-dedicated research programs. Managing medical monitoring, protocol execution, data review, and investigator collaboration.
Lead Business Operations Specialist
RBQM Lead overseeing risk-based quality management for ICON’s global clinical research studies. Driving risk assessments, monitoring strategies, governance, and inspection readiness across clinical trials.
Study Site Management Specialist
Site Activation Lead managing clinical trial start-up and site activation for ICON's sponsor-dedicated clinical research services. Overseeing regulatory submissions, activation plans, project delivery, and sponsor communications.
Clinical Data Risk Analyst, Mandarin Speaker
Clinical Data Risk Analyst at ICON, a global healthcare intelligence and clinical research organization. Assessing clinical-trial data risks, quality, integrity, and regulatory compliance.
Site Care Partner
Remote Site Care Partner supporting UK clinical trial sites for ICON Strategic Solutions. Building site relationships, guiding compliance, and optimizing study engagement with reduced travel.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON. Ensuring protocol compliance, site performance, data integrity, and regulatory standards.
Clinical Operations Manager
Clinical Operations Manager overseeing country budgets, submissions, compliance and site readiness in Madrid. Supporting ICON’s sponsor-dedicated clinical research operations and trial start-up.
Medical Operations Associate
Medical Operations Associate supporting medical monitoring and drug development projects at ICON, a global healthcare intelligence and clinical research organisation. Coordinating stakeholders, quality control, mentoring, and process improvement.
Site Activation Partner
Site Activation Partner launching clinical trials for ICON’s sponsor-dedicated research programs. Coordinating regulatory submissions, approvals, and study-startup documentation.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring respiratory and cardiovascular clinical trials for ICON in the Greater Toronto Area. Overseeing sites, compliance, data integrity, and trial execution.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring sponsor-dedicated Phase I oncology trials at ICON. Managing sites, ensuring GCP compliance, and guiding clinical trial teams.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing remote Phase I oncology trial monitoring for ICON Strategic Solutions. Managing sites, compliance, data integrity, and CRA guidance.
Clinical Trial Manager
Clinical Trial Manager managing timelines, quality, vendors, and stakeholders for ICON’s sponsor-dedicated clinical research programs. Supporting trials that advance patient treatments.
Project Manager
Pharmacovigilance Project Manager leading clinical-trial and post-marketing drug-safety projects at ICON. Coordinating regulatory submissions, cross-functional teams, risks, and project delivery.
Client Services Associate II
Client Services Associate managing Clinical Outcome Assessment licensing and translation services for ICON. Coordinating client proposals, projects, contracts, and delivery across global healthcare research.
Clinical Trial Assistant
Clinical Trial Assistant supporting clinical trial coordination and documentation at ICON Strategic Solutions. Contributing to compliant trial execution and development of innovative treatments.
Site Contract and Budget Specialist
Site Contract and Budget Specialist managing clinical-trial contracts for ICON’s sponsor-dedicated research services. Negotiating vendor agreements and mitigating contractual risks.